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minoxidil
minoxidil - 37808-798-30 - (Minoxidil)
Drug Information of minoxidil
| Product NDC: | 37808-798 |
| Proprietary Name: | minoxidil |
| Non Proprietary Name: | Minoxidil |
| Active Ingredient(s): | 3 g/60mL & nbsp; Minoxidil |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of minoxidil
| Product NDC: | 37808-798 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075598 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100216 |
Package Information of minoxidil
| Package NDC: | 37808-798-30 |
| Package Description: | 3 BOTTLE in 1 CARTON (37808-798-30) > 60 mL in 1 BOTTLE |
NDC Information of minoxidil
| NDC Code | 37808-798-30 |
| Proprietary Name | minoxidil |
| Package Description | 3 BOTTLE in 1 CARTON (37808-798-30) > 60 mL in 1 BOTTLE |
| Product NDC | 37808-798 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Minoxidil |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100216 |
| Marketing Category Name | ANDA |
| Labeler Name | H E B |
| Substance Name | MINOXIDIL |
| Strength Number | 3 |
| Strength Unit | g/60mL |
| Pharmaceutical Classes |
