| NDC Code | 68462-433-90 |
|---|
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (68462-433-90) |
|---|
| Product NDC | 68462-433 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Colesevelam Hydrochloride |
|---|
| Non-Proprietary Name | Colesevelam Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20180518 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA203480 |
|---|
| Manufacturer | Glenmark Pharmaceuticals Inc., USA |
|---|
| Substance Name | COLESEVELAM HYDROCHLORIDE |
|---|
| Strength | 625 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Bile Acid Sequestrant [EPC], Bile-acid Binding Activity [MoA] |
|---|