NDC 54868-4120 Propecia
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-4120 - Propecia
Product Characteristics
Product Packages
NDC Code 54868-4120-0
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE
NDC Code 54868-4120-1
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 54868-4120?
What are the uses for Propecia?
Which are Propecia UNII Codes?
The UNII codes for the active ingredients in this product are:
- FINASTERIDE (UNII: 57GNO57U7G)
- FINASTERIDE (UNII: 57GNO57U7G) (Active Moiety)
Which are Propecia 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:
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- STARCH, CORN (UNII: O8232NY3SJ)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- HYDROXYPROPYL CELLULOSE (TYPE H) (UNII: RFW2ET671P)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- TALC (UNII: 7SEV7J4R1U)
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
What is the NDC to RxNorm Crosswalk for Propecia?
- RxCUI: 200172 - finasteride 1 MG Oral Tablet
- RxCUI: 200172 - FIN5C 1 MG Oral Tablet
- RxCUI: 213178 - Propecia 1 MG Oral Tablet
- RxCUI: 213178 - finasteride 1 MG Oral Tablet [Propecia]
- RxCUI: 213178 - FIN5C 1 MG Oral Tablet [Propecia]
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[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".