| NDC Code | 14789-202-05 |
|---|
| Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (14789-202-05) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (14789-202-07) |
|---|
| Product NDC | 14789-202 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Minocycline Hydrochloride |
|---|
| Non-Proprietary Name | Minocycline Hydrochloride |
|---|
| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20221219 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA214934 |
|---|
| Manufacturer | Nexus Pharmaceuticals Inc. |
|---|
| Substance Name | MINOCYCLINE HYDROCHLORIDE |
|---|
| Strength | 100 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Tetracycline-class Drug [EPC], Tetracyclines [CS] |
|---|