Nateglinide is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Zydus Pharmaceuticals (usa) Inc.. The primary component is Nateglinide.
| Product ID | 68382-722_716586d5-0843-4613-84a9-ea1c972229ff |
| NDC | 68382-722 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Nateglinide |
| Generic Name | Nateglinide |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2016-10-27 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA205248 |
| Labeler Name | Zydus Pharmaceuticals (USA) Inc. |
| Substance Name | NATEGLINIDE |
| Active Ingredient Strength | 120 mg/1 |
| Pharm Classes | Glinide [EPC],Potassium Channel Antagonists [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2016-10-27 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA205248 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-10-27 |
| Marketing Category | ANDA |
| Application Number | ANDA205248 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-10-27 |
| Marketing Category | ANDA |
| Application Number | ANDA205248 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2016-10-27 |
| Marketing Category | ANDA |
| Application Number | ANDA205248 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-10-27 |
| Marketing Category | ANDA |
| Application Number | ANDA205248 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-10-27 |
| Marketing Category | ANDA |
| Application Number | ANDA205248 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-10-27 |
| Marketing End Date | 2018-12-20 |
| Marketing Category | ANDA |
| Application Number | ANDA205248 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-10-27 |
| Ingredient | Strength |
|---|---|
| NATEGLINIDE | 120 mg/1 |
| SPL SET ID: | 88698921-cd8f-4d41-96e6-ff671913c5c3 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0591-3354 | Nateglinide | Nateglinide |
| 0591-3355 | Nateglinide | Nateglinide |
| 0615-7585 | Nateglinide | Nateglinide |
| 0615-7586 | Nateglinide | Nateglinide |
| 16571-758 | NATEGLINIDE | NATEGLINIDE |
| 16571-759 | NATEGLINIDE | NATEGLINIDE |
| 42291-636 | Nateglinide | Nateglinide |
| 42291-637 | Nateglinide | Nateglinide |
| 49884-984 | Nateglinide | Nateglinide |
| 49884-985 | Nateglinide | Nateglinide |
| 51407-656 | Nateglinide | nateglinide |
| 51407-657 | Nateglinide | nateglinide |
| 52536-063 | Nateglinide | Nateglinide |
| 52536-067 | Nateglinide | Nateglinide |
| 55111-328 | Nateglinide | Nateglinide |
| 55111-329 | Nateglinide | Nateglinide |
| 60429-434 | Nateglinide | Nateglinide |
| 60429-435 | Nateglinide | Nateglinide |
| 60687-673 | Nateglinide | nateglinide |
| 60687-684 | Nateglinide | nateglinide |
| 64380-167 | Nateglinide | nateglinide |
| 64380-168 | Nateglinide | nateglinide |
| 68084-458 | Nateglinide | Nateglinide |
| 68084-459 | Nateglinide | Nateglinide |
| 68382-721 | Nateglinide | Nateglinide |
| 68382-722 | Nateglinide | Nateglinide |
| 70771-1016 | Nateglinide | Nateglinide |
| 70771-1015 | Nateglinide | Nateglinide |
| 71209-030 | Nateglinide | Nateglinide |
| 71209-031 | Nateglinide | Nateglinide |
| 75834-205 | NATEGLINIDE | NATEGLINIDE |
| 75834-206 | NATEGLINIDE | NATEGLINIDE |
| 0078-0351 | Starlix | nateglinide |
| 0078-0352 | Starlix | nateglinide |