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Prandin
Prandin - 54868-5381-0 - (repaglinide)
Drug Information of Prandin
| Product NDC: | 54868-5381 |
| Proprietary Name: | Prandin |
| Non Proprietary Name: | repaglinide |
| Active Ingredient(s): | 2 mg/1 & nbsp; repaglinide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Prandin
| Product NDC: | 54868-5381 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020741 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20050808 |
Package Information of Prandin
| Package NDC: | 54868-5381-0 |
| Package Description: | 10 TABLET in 1 BOTTLE, PLASTIC (54868-5381-0) |
NDC Information of Prandin
| NDC Code | 54868-5381-0 |
| Proprietary Name | Prandin |
| Package Description | 10 TABLET in 1 BOTTLE, PLASTIC (54868-5381-0) |
| Product NDC | 54868-5381 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | repaglinide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20050808 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | REPAGLINIDE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Glinide [EPC],Potassium Channel Antagonists [MoA] |
