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MINOCYCLINE HYDROCHLORIDE
MINOCYCLINE HYDROCHLORIDE - 0115-7018-13 - (MINOCYCLINE HYDROCHLORIDE)
Drug Information of MINOCYCLINE HYDROCHLORIDE
| Product NDC: | 0115-7018 |
| Proprietary Name: | MINOCYCLINE HYDROCHLORIDE |
| Non Proprietary Name: | MINOCYCLINE HYDROCHLORIDE |
| Active Ingredient(s): | 100 mg/1 & nbsp; MINOCYCLINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MINOCYCLINE HYDROCHLORIDE
| Product NDC: | 0115-7018 |
| Labeler Name: | Global Pharmaceuticals, Division of Impax Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065005 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19990323 |
Package Information of MINOCYCLINE HYDROCHLORIDE
| Package NDC: | 0115-7018-13 |
| Package Description: | 60 CAPSULE in 1 BOTTLE (0115-7018-13) |
NDC Information of MINOCYCLINE HYDROCHLORIDE
| NDC Code | 0115-7018-13 |
| Proprietary Name | MINOCYCLINE HYDROCHLORIDE |
| Package Description | 60 CAPSULE in 1 BOTTLE (0115-7018-13) |
| Product NDC | 0115-7018 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | MINOCYCLINE HYDROCHLORIDE |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19990323 |
| Marketing Category Name | ANDA |
| Labeler Name | Global Pharmaceuticals, Division of Impax Laboratories Inc. |
| Substance Name | MINOCYCLINE HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient] |
