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Minoxidil
Minoxidil - 50383-001-20 - (Minoxidil)
Drug Information of Minoxidil
| Product NDC: | 50383-001 |
| Proprietary Name: | Minoxidil |
| Non Proprietary Name: | Minoxidil |
| Active Ingredient(s): | 2 g/100mL & nbsp; Minoxidil |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Minoxidil
| Product NDC: | 50383-001 |
| Labeler Name: | Hi-Tech Pharmacal Co., Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA074731 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19961224 |
Package Information of Minoxidil
| Package NDC: | 50383-001-20 |
| Package Description: | 1 BOTTLE in 1 CARTON (50383-001-20) > 60 mL in 1 BOTTLE |
NDC Information of Minoxidil
| NDC Code | 50383-001-20 |
| Proprietary Name | Minoxidil |
| Package Description | 1 BOTTLE in 1 CARTON (50383-001-20) > 60 mL in 1 BOTTLE |
| Product NDC | 50383-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Minoxidil |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19961224 |
| Marketing Category Name | ANDA |
| Labeler Name | Hi-Tech Pharmacal Co., Inc. |
| Substance Name | MINOXIDIL |
| Strength Number | 2 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
