| NDC Code | 68382-535-30 |
|---|
| Package Description | 10 BLISTER PACK in 1 CARTON (68382-535-30) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
|---|
| Product NDC | 68382-535 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Minocycline Hydrochloride |
|---|
| Non-Proprietary Name | Minocycline Hydrochloride |
|---|
| Dosage Form | TABLET, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20180307 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA203553 |
|---|
| Manufacturer | Zydus Pharmaceuticals (USA) Inc. |
|---|
| Substance Name | MINOCYCLINE HYDROCHLORIDE |
|---|
| Strength | 135 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Decreased Prothrombin Activity [PE], Tetracycline-class Drug [EPC], Tetracyclines [CS] |
|---|