WOMENS alopexy
- Product NDC
- 64760-601
- 11-digit product format
- 647600601
- Labeler code
- 64760
- Product ID
- 64760-601_7e53ed01-78a7-1354-e053-2a91aa0ae6f3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- minoxidil
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Genesis Pharmaceutical, Inc.
- Application
- ANDA078176
- Marketing category
- ANDA
- Marketing start
- 2016-08-08
- Marketing end
- 2019-09-11
- Substance
- MINOXIDIL
- Active strength
- 20 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record