Details for New Drug Application (NDA): 075357
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The generic ingredient in MINOXIDIL (FOR WOMEN) is minoxidil. There are eight drug master file entries for this compound. Eighty-six suppliers are listed for this compound. Additional details are available on the minoxidil profile page.
Summary for 075357
Tradename: | MINOXIDIL (FOR WOMEN) |
Applicant: | L Perrigo Co |
Ingredient: | minoxidil |
Patents: | 0 |
Pharmacology for NDA: 075357
Physiological Effect | Arteriolar Vasodilation |
Medical Subject Heading (MeSH) Categories for 075357
Suppliers and Packaging for NDA: 075357
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
MINOXIDIL (FOR MEN) | minoxidil | SOLUTION;TOPICAL | 075357 | ANDA | Walgreen Company | 0363-0703 | 0363-0703-16 | 1 BOTTLE, DROPPER in 1 CARTON (0363-0703-16) / 60 mL in 1 BOTTLE, DROPPER |
MINOXIDIL (FOR MEN) | minoxidil | SOLUTION;TOPICAL | 075357 | ANDA | Walgreen Company | 0363-0703 | 0363-0703-30 | 3 BOTTLE, DROPPER in 1 CARTON (0363-0703-30) / 60 mL in 1 BOTTLE, DROPPER |
Profile for product number 001
Active Rx/OTC/Discontinued: | OTC | Dosage: | SOLUTION;TOPICAL | Strength | 2% | ||||
Approval Date: | Jul 30, 1999 | TE: | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | OTC | Dosage: | SOLUTION;TOPICAL | Strength | 2% | ||||
Approval Date: | Jul 30, 1999 | TE: | RLD: | No |
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