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up and up minoxidil
up and up minoxidil - 11673-380-16 - (Minoxidil)
Drug Information of up and up minoxidil
| Product NDC: | 11673-380 |
| Proprietary Name: | up and up minoxidil |
| Non Proprietary Name: | Minoxidil |
| Active Ingredient(s): | 5 g/100mL & nbsp; Minoxidil |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of up and up minoxidil
| Product NDC: | 11673-380 |
| Labeler Name: | Target Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075598 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090520 |
Package Information of up and up minoxidil
| Package NDC: | 11673-380-16 |
| Package Description: | 1 BOTTLE in 1 CARTON (11673-380-16) > 60 mL in 1 BOTTLE |
NDC Information of up and up minoxidil
| NDC Code | 11673-380-16 |
| Proprietary Name | up and up minoxidil |
| Package Description | 1 BOTTLE in 1 CARTON (11673-380-16) > 60 mL in 1 BOTTLE |
| Product NDC | 11673-380 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Minoxidil |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20090520 |
| Marketing Category Name | ANDA |
| Labeler Name | Target Corporation |
| Substance Name | MINOXIDIL |
| Strength Number | 5 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
