Product NDC: | 49884-984 |
Proprietary Name: | Nateglinide |
Non Proprietary Name: | Nateglinide |
Active Ingredient(s): | 60 mg/1 & nbsp; Nateglinide |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49884-984 |
Labeler Name: | Par Pharmaceutical Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077463 |
Marketing Category: | ANDA |
Start Marketing Date: | 20090908 |
Package NDC: | 49884-984-10 |
Package Description: | 1000 TABLET, COATED in 1 BOTTLE, PLASTIC (49884-984-10) |
NDC Code | 49884-984-10 |
Proprietary Name | Nateglinide |
Package Description | 1000 TABLET, COATED in 1 BOTTLE, PLASTIC (49884-984-10) |
Product NDC | 49884-984 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Nateglinide |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20090908 |
Marketing Category Name | ANDA |
Labeler Name | Par Pharmaceutical Inc. |
Substance Name | NATEGLINIDE |
Strength Number | 60 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Glinide [EPC],Potassium Channel Antagonists [MoA] |