NDC 53808-0734 Minoxidil
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53808 - Doh Central Pharmacy
- 53808-0734 - Minoxidil
Product Characteristics
Product Packages
NDC Code 53808-0734-1
Package Description: 30 TABLET in 1 BLISTER PACK
Product Details
What is NDC 53808-0734?
What are the uses for Minoxidil?
Which are Minoxidil UNII Codes?
The UNII codes for the active ingredients in this product are:
- MINOXIDIL (UNII: 5965120SH1)
- MINOXIDIL (UNII: 5965120SH1) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Minoxidil?
- RxCUI: 197986 - minoxidil 10 MG Oral Tablet
- RxCUI: 197987 - minoxidil 2.5 MG Oral Tablet
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[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".