Product NDC: | 0472-0094 |
Proprietary Name: | Hair Regrowth Treatment For Men |
Non Proprietary Name: | minoxidil |
Active Ingredient(s): | 50 mg/mL & nbsp; minoxidil |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0472-0094 |
Labeler Name: | Actavis Mid Atlantic LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA075518 |
Marketing Category: | ANDA |
Start Marketing Date: | 20001117 |
Package NDC: | 0472-0094-75 |
Package Description: | 2 BOTTLE in 1 CARTON (0472-0094-75) > 60 mL in 1 BOTTLE |
NDC Code | 0472-0094-75 |
Proprietary Name | Hair Regrowth Treatment For Men |
Package Description | 2 BOTTLE in 1 CARTON (0472-0094-75) > 60 mL in 1 BOTTLE |
Product NDC | 0472-0094 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | minoxidil |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20001117 |
Marketing Category Name | ANDA |
Labeler Name | Actavis Mid Atlantic LLC |
Substance Name | MINOXIDIL |
Strength Number | 50 |
Strength Unit | mg/mL |
Pharmaceutical Classes |