0078-0351 : Starlix 60 mg Oral Tablet
| NDC: | 0078-0351 |
| Labeler: | Novartis Pharmaceuticals Corporation |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Starlix |
| Dosage Form: | Oral Tablet |
| Application #: | NDA021204 |
| Rev. Date: |
Appearance:
| Markings: | STARLIX;60 |
| Shapes: |
Round |
| Colors: |
 Pink |
| Size (mm): | 10 |
| Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. | |
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.
NDC Package Codes:
- 0078-0351-05: 100 TABLET IN 1 BOTTLE (0078‑0351‑05)
Active Ingredients:
- Nateglinide
Dosage Strength:
- 60 mg
Inactive Ingredients:
- Silicon Dioxide
- Croscarmellose Sodium
- Hypromellose 2208 (15000 Mpa.s)
- Lactose Monohydrate
- Magnesium Stearate
- Cellulose, Microcrystalline
- Polyethylene Glycols
- Povidones
- Talc
- Titanium Dioxide
- Ferric Oxide Red
Pharmaceutical Classes:
- Glinide [EPC]
- Potassium Channel Antagonists [MoA]
Related Products:
Based on records with the same trade name.- 0078-0352 Starlix 120 mg Oral Tablet by Novartis Pharmaceuticals Corporation
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.