| NDC Code | 62584-163-65 |
|---|
| Package Description | 50 BLISTER PACK in 1 BOX, UNIT-DOSE (62584-163-65) / 1 TABLET in 1 BLISTER PACK (62584-163-11) |
|---|
| Product NDC | 62584-163 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Demeclocycline Hydrochloride |
|---|
| Non-Proprietary Name | Demeclocycline Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20101209 |
|---|
| End Marketing Date | 20231031 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA065425 |
|---|
| Manufacturer | American Health Packaging |
|---|
| Substance Name | DEMECLOCYCLINE HYDROCHLORIDE |
|---|
| Strength | 300 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Tetracycline-class Antimicrobial [EPC], Tetracyclines [CS] |
|---|