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Nateglinide
Nateglinide - 68084-459-21 - (Nateglinide)
Drug Information of Nateglinide
| Product NDC: | 68084-459 |
| Proprietary Name: | Nateglinide |
| Non Proprietary Name: | Nateglinide |
| Active Ingredient(s): | 120 mg/1 & nbsp; Nateglinide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nateglinide
| Product NDC: | 68084-459 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077463 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120102 |
Package Information of Nateglinide
| Package NDC: | 68084-459-21 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (68084-459-21) > 10 TABLET, COATED in 1 BLISTER PACK (68084-459-11) |
NDC Information of Nateglinide
| NDC Code | 68084-459-21 |
| Proprietary Name | Nateglinide |
| Package Description | 3 BLISTER PACK in 1 CARTON (68084-459-21) > 10 TABLET, COATED in 1 BLISTER PACK (68084-459-11) |
| Product NDC | 68084-459 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nateglinide |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120102 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | NATEGLINIDE |
| Strength Number | 120 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Glinide [EPC],Potassium Channel Antagonists [MoA] |
