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Minocycline
Minocycline - 49884-512-01 - (Minocycline)
Drug Information of Minocycline
| Product NDC: | 49884-512 |
| Proprietary Name: | Minocycline |
| Non Proprietary Name: | Minocycline |
| Active Ingredient(s): | 75 mg/1 & nbsp; Minocycline |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Minocycline
| Product NDC: | 49884-512 |
| Labeler Name: | Par Pharmaceutical, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065131 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030416 |
Package Information of Minocycline
| Package NDC: | 49884-512-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (49884-512-01) |
NDC Information of Minocycline
| NDC Code | 49884-512-01 |
| Proprietary Name | Minocycline |
| Package Description | 100 TABLET in 1 BOTTLE (49884-512-01) |
| Product NDC | 49884-512 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Minocycline |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20030416 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical, Inc. |
| Substance Name | MINOCYCLINE HYDROCHLORIDE |
| Strength Number | 75 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient] |
