Details for New Drug Application (NDA): 206432
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The generic ingredient in NATEGLINIDE is nateglinide. There are nine drug master file entries for this compound. Eleven suppliers are listed for this compound. Additional details are available on the nateglinide profile page.
Summary for 206432
| Tradename: | NATEGLINIDE |
| Applicant: | Cadila Pharms Ltd |
| Ingredient: | nateglinide |
| Patents: | 0 |
Pharmacology for NDA: 206432
| Mechanism of Action | Potassium Channel Antagonists |
Suppliers and Packaging for NDA: 206432
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| NATEGLINIDE | nateglinide | TABLET;ORAL | 206432 | ANDA | Cadila Pharmaceuticals Limited | 71209-030 | 71209-030-04 | 90 TABLET, COATED in 1 BOTTLE (71209-030-04) |
| NATEGLINIDE | nateglinide | TABLET;ORAL | 206432 | ANDA | Cadila Pharmaceuticals Limited | 71209-030 | 71209-030-05 | 100 TABLET, COATED in 1 BOTTLE (71209-030-05) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 60MG | ||||
| Approval Date: | Apr 19, 2019 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 120MG | ||||
| Approval Date: | Apr 19, 2019 | TE: | AB | RLD: | No | ||||
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