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. One hundred and five 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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