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Niacor
Niacor - 0245-0067-11 - (niacin)
Drug Information of Niacor
| Product NDC: | 0245-0067 |
| Proprietary Name: | Niacor |
| Non Proprietary Name: | niacin |
| Active Ingredient(s): | 500 mg/1 & nbsp; niacin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Niacor
| Product NDC: | 0245-0067 |
| Labeler Name: | Upsher-Smith Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040378 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20000503 |
Package Information of Niacor
| Package NDC: | 0245-0067-11 |
| Package Description: | 100 TABLET in 1 BOTTLE (0245-0067-11) |
NDC Information of Niacor
| NDC Code | 0245-0067-11 |
| Proprietary Name | Niacor |
| Package Description | 100 TABLET in 1 BOTTLE (0245-0067-11) |
| Product NDC | 0245-0067 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | niacin |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20000503 |
| Marketing Category Name | ANDA |
| Labeler Name | Upsher-Smith Laboratories Inc. |
| Substance Name | NIACIN |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Nicotinic Acid [EPC],Nicotinic Acids [Chemical/Ingredient] |
