| Drug NDC: | 51885-7070 |
| 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: | Pseudognaphalium Obtusifolium And Causticum And Colchicum Autumnale Bulb And Citrullus Colocynthis Fruit Pulp And Iron And Lithium Benzoate And Toxicodendron Pubescens Leaf And Filipendula Ulmaria Root |
| Also known as the trade name. It is the name of the product chosen by the labeler. | |
| Product Type: | Bulk Ingredient |
| 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: | Pseudognaphalium Obtusifolium And Causticum And Colchicum Autumnale Bulb And Citrullus Colocynthis Fruit Pulp And Iron And Lithium Benzoate And Toxicodendron Pubescens Leaf And Filipendula Ulmaria Root |
| Also known as the generic name, this is usually the active ingredient(s) of the product. | |
| Labeler Name: | Biologische Heilmittel Heel |
| Name of Company corresponding to the labeler code segment of the ProductNDC. | |
| Dosage Form: | Injection |
| 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: | Unfinished |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. | |
| Substance Name: | CAUSTICUM - 10 [hp_X]/1.1mL CITRULLUS COLOCYNTHIS FRUIT PULP - 10 [hp_X]/1.1mL COLCHICUM AUTUMNALE BULB - 10 [hp_X]/1.1mL FILIPENDULA ULMARIA ROOT - 10 [hp_X]/1.1mL IRON - 10 [hp_X]/1.1mL LITHIUM BENZOATE - 10 [hp_X]/1.1mL PSEUDOGNAPHALIUM OBTUSIFOLIUM - 6 [hp_X]/1.1mL TOXICODENDRON PUBESCENS LEAF - 10 [hp_X]/1.1mL |
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. | |
| Route Details: | |
| 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 Category: | DRUG FOR FURTHER PROCESSING |
| 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: | 31 Mar, 2018 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. | |
| Marketing End Date: | 31 Aug, 2023 |
| 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: | 27 Dec, 2025 |
| This is the date when the listing record will expire if not updated or certified by the firm. | |
| Manufacturer Name: | |
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. | |
| UNII: | |
| 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. | |
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|---|---|---|---|
| 51885-7070-1 | 1000 AMPULE in 1 BOX (51885-7070-1) / 1.1 mL in 1 AMPULE | 31 Mar, 2018 | 31 Aug, 2023 | No |
| 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. | ||||
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