Multivitamin With Fluoride

.alpha.-tocopherol Acetate, Dl-, Ascorbic Acid, Cyanocobalamin, Folic Acid, Niacin, Pyridoxine, Riboflavin, Sodium Fluoride, Thiamine Mononitrate, Vitamin A And Vitamin D


Bryant Ranch Prepack
Human Prescription Drug
NDC 63629-1135
Multivitamin With Fluoride also known as .alpha.-tocopherol Acetate, Dl-, Ascorbic Acid, Cyanocobalamin, Folic Acid, Niacin, Pyridoxine, Riboflavin, Sodium Fluoride, Thiamine Mononitrate, Vitamin A And Vitamin D is a human prescription drug labeled by 'Bryant Ranch Prepack'. National Drug Code (NDC) number for Multivitamin With Fluoride is 63629-1135. This drug is available in dosage form of Tablet, Chewable. The names of the active, medicinal ingredients in Multivitamin With Fluoride drug includes .alpha.-tocopherol Acetate, Dl- - 15 [iU]/1 Ascorbic Acid - 60 mg/1 Cyanocobalamin - 4.5 ug/1 Folic Acid - 300 ug/1 Niacin - 13.5 mg/1 Pyridoxine - 1.05 mg/1 Riboflavin - 1.2 mg/1 Sodium Fluoride - .25 mg/1 Thiamine Mononitrate - 1.05 mg/1 Vitamin A - 2500 [iU]/1 and more. The currest status of Multivitamin With Fluoride drug is Active.

Drug Information:

Drug NDC: 63629-1135
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name: Multivitamin With Fluoride
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type: Human Prescription Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name: .alpha.-tocopherol Acetate, Dl-, Ascorbic Acid, Cyanocobalamin, Folic Acid, Niacin, Pyridoxine, Riboflavin, Sodium Fluoride, Thiamine Mononitrate, Vitamin A And Vitamin D
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Bryant Ranch Prepack
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Tablet, Chewable
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status: Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:.ALPHA.-TOCOPHEROL ACETATE, DL- - 15 [iU]/1
ASCORBIC ACID - 60 mg/1
CYANOCOBALAMIN - 4.5 ug/1
FOLIC ACID - 300 ug/1
NIACIN - 13.5 mg/1
PYRIDOXINE - 1.05 mg/1
RIBOFLAVIN - 1.2 mg/1
SODIUM FLUORIDE - .25 mg/1
THIAMINE MONONITRATE - 1.05 mg/1
VITAMIN A - 2500 [iU]/1
VITAMIN D - 400 [iU]/1
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Marketing Category: UNAPPROVED DRUG OTHER
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Marketing Start Date: 20 Jul, 2018
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 20 Dec, 2025
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Listing Expiration Date: 31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Manufacturer Name:Bryant Ranch Prepack
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
NUI:N0000193618
M0001797
M0022794
N0000175951
N0000175594
M0014839
N0000192800
N0000005657
N0000175452
M0022788
N0000175950
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:WR1WPI7EW8
PQ6CK8PD0R
P6YC3EG204
935E97BOY8
2679MF687A
KV2JZ1BI6Z
TLM2976OFR
8ZYQ1474W7
8K0I04919X
81G40H8B0T
9VU1KI44GP
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class EPC:Vitamin C [EPC]
Vitamin B12 [EPC]
Nicotinic Acid [EPC]
Vitamin B6 Analog [EPC]
Vitamin A [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class CS:Ascorbic Acid [CS]
Vitamin B 12 [CS]
Nicotinic Acids [CS]
Vitamin B 6 [Chemical/Ingredient]
Analogs/Derivatives [Chemical/Ingredient]
Vitamin A [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:Analogs/Derivatives [Chemical/Ingredient]
Ascorbic Acid [CS]
Nicotinic Acid [EPC]
Nicotinic Acids [CS]
Vitamin A [CS]
Vitamin A [EPC]
Vitamin B 12 [CS]
Vitamin B 6 [Chemical/Ingredient]
Vitamin B12 [EPC]
Vitamin B6 Analog [EPC]
Vitamin C [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
63629-1135-190 TABLET, CHEWABLE in 1 BOTTLE (63629-1135-1)20 Jul, 2018N/ANo
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.