| NDC Code | 65862-558-99 |
|---|
| Package Description | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-558-99) |
|---|
| Product NDC | 65862-558 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Minocycline Hydrochloride |
|---|
| Non-Proprietary Name | Minocycline Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20121119 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA202261 |
|---|
| Manufacturer | Aurobindo Pharma Limited |
|---|
| Substance Name | MINOCYCLINE HYDROCHLORIDE |
|---|
| Strength | 135 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Decreased Prothrombin Activity [PE], Tetracycline-class Drug [EPC], Tetracyclines [CS] |
|---|