| NDC Code | 54868-0017-1 |
|---|
| Package Description | 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (54868-0017-1) |
|---|
| Product NDC | 54868-0017 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Niaspan |
|---|
| Non-Proprietary Name | Niacin |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20090512 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA020381 |
|---|
| Manufacturer | Physicians Total Care, Inc. |
|---|
| Substance Name | NIACIN |
|---|
| Strength | 1000 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Nicotinic Acid [EPC],Nicotinic Acids [Chemical/Ingredient] |
|---|