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MINOXIDIL
MINOXIDIL - 53808-0734-1 - (minoxidil)
Drug Information of MINOXIDIL
| Product NDC: | 53808-0734 |
| Proprietary Name: | MINOXIDIL |
| Non Proprietary Name: | minoxidil |
| Active Ingredient(s): | 2.5 mg/1 & nbsp; minoxidil |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MINOXIDIL
| Product NDC: | 53808-0734 |
| Labeler Name: | State of Florida DOH Central Pharmacy |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072709 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090701 |
Package Information of MINOXIDIL
| Package NDC: | 53808-0734-1 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (53808-0734-1) |
NDC Information of MINOXIDIL
| NDC Code | 53808-0734-1 |
| Proprietary Name | MINOXIDIL |
| Package Description | 30 TABLET in 1 BLISTER PACK (53808-0734-1) |
| Product NDC | 53808-0734 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | minoxidil |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090701 |
| Marketing Category Name | ANDA |
| Labeler Name | State of Florida DOH Central Pharmacy |
| Substance Name | MINOXIDIL |
| Strength Number | 2.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC] |
