NDC 36987-1041 Gerbil Epithelium
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 36987-1041?
What are the uses for Gerbil Epithelium?
Which are Gerbil Epithelium UNII Codes?
The UNII codes for the active ingredients in this product are:
- BOS TAURUS SKIN (UNII: 7J12CD6O9L)
- BOS TAURUS SKIN (UNII: 7J12CD6O9L) (Active Moiety)
- CANIS LUPUS FAMILIARIS SKIN (UNII: X2W7CLE97T)
- CANIS LUPUS FAMILIARIS SKIN (UNII: X2W7CLE97T) (Active Moiety)
- GALLUS GALLUS FEATHER (UNII: 1FCM16V0FV)
- GALLUS GALLUS FEATHER (UNII: 1FCM16V0FV) (Active Moiety)
- ANAS PLATYRHYNCHOS FEATHER (UNII: 83B65P4796)
- ANAS PLATYRHYNCHOS FEATHER (UNII: 83B65P4796) (Active Moiety)
- ANSER ANSER FEATHER (UNII: 15XI414745)
- ANSER ANSER FEATHER (UNII: 15XI414745) (Active Moiety)
- MERIONES UNGUICULATUS SKIN (UNII: 9WN2H714TG)
- MERIONES UNGUICULATUS SKIN (UNII: 9WN2H714TG) (Active Moiety)
Which are Gerbil Epithelium Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- PHENOL (UNII: 339NCG44TV)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Gerbil Epithelium?
- RxCUI: 889658 - hog skin extract 10000 UNT/mL Injectable Solution
- RxCUI: 889658 - hog skin extract 10000 UNT/ML Injectable Solution
- RxCUI: 889658 - Sus scrofa skin extract 10,000 UNT/ML Injectable Solution
- RxCUI: 894776 - duck feather extract 10,000 UNT/mL Injectable Solution
- RxCUI: 894776 - duck feather extract 10000 UNT/ML Injectable Solution
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/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.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".