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Minoxidil
Minoxidil - 52125-039-02 - (Minoxidil)
Drug Information of Minoxidil
| Product NDC: | 52125-039 |
| Proprietary Name: | Minoxidil |
| Non Proprietary Name: | Minoxidil |
| Active Ingredient(s): | 10 mg/1 & nbsp; Minoxidil |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Minoxidil
| Product NDC: | 52125-039 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA071839 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130226 |
Package Information of Minoxidil
| Package NDC: | 52125-039-02 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (52125-039-02) |
NDC Information of Minoxidil
| NDC Code | 52125-039-02 |
| Proprietary Name | Minoxidil |
| Package Description | 30 TABLET in 1 BLISTER PACK (52125-039-02) |
| Product NDC | 52125-039 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Minoxidil |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130226 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | MINOXIDIL |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC] |
