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Minocycline Hydrochloride
Minocycline Hydrochloride - 68180-381-06 - (Minocycline Hydrochloride)
Drug Information of Minocycline Hydrochloride
| Product NDC: | 68180-381 |
| Proprietary Name: | Minocycline Hydrochloride |
| Non Proprietary Name: | Minocycline Hydrochloride |
| Active Ingredient(s): | 135 mg/1 & nbsp; Minocycline Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Minocycline Hydrochloride
| Product NDC: | 68180-381 |
| Labeler Name: | LUPIN PHARMACEUTICALS INC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091424 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120214 |
Package Information of Minocycline Hydrochloride
| Package NDC: | 68180-381-06 |
| Package Description: | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-381-06) |
NDC Information of Minocycline Hydrochloride
| NDC Code | 68180-381-06 |
| Proprietary Name | Minocycline Hydrochloride |
| Package Description | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-381-06) |
| Product NDC | 68180-381 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Minocycline Hydrochloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20120214 |
| Marketing Category Name | ANDA |
| Labeler Name | LUPIN PHARMACEUTICALS INC |
| Substance Name | MINOCYCLINE HYDROCHLORIDE |
| Strength Number | 135 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient] |
