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Minocin
Minocin - 14290-501-88 - (minocycline hydrochloride)
Drug Information of Minocin
| Product NDC: | 14290-501 |
| Proprietary Name: | Minocin |
| Non Proprietary Name: | minocycline hydrochloride |
| Active Ingredient(s): | 50 mg/1 & nbsp; minocycline hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, COATED PELLETS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Minocin
| Product NDC: | 14290-501 |
| Labeler Name: | Triax Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050649 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20070901 |
Package Information of Minocin
| Package NDC: | 14290-501-88 |
| Package Description: | 100 CAPSULE, COATED PELLETS in 1 BOTTLE (14290-501-88) |
NDC Information of Minocin
| NDC Code | 14290-501-88 |
| Proprietary Name | Minocin |
| Package Description | 100 CAPSULE, COATED PELLETS in 1 BOTTLE (14290-501-88) |
| Product NDC | 14290-501 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | minocycline hydrochloride |
| Dosage Form Name | CAPSULE, COATED PELLETS |
| Route Name | ORAL |
| Start Marketing Date | 20070901 |
| Marketing Category Name | NDA |
| Labeler Name | Triax Pharmaceuticals, LLC |
| Substance Name | MINOCYCLINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient] |
