48792-7865 : Linagliptin 5 mg Oral Tablet, Film Coated
| NDC: | 48792-7865 |
| Labeler: | Sunshine Lake Pharma Co., Ltd. |
| Product Type: | Human Prescription Drug |
| Drug Name: | Linagliptin |
| Dosage Form: | Oral Tablet, Film Coated |
| Application #: | ANDA208335 |
| Rev. Date: |
NDC Package Codes:
- 48792-7865-1: 30 TABLET, FILM COATED IN 1 BOTTLE (48792‑7865‑1)
Active Ingredients:
- Linagliptin
Dosage Strength:
- 5 mg
Pharmaceutical Classes:
- Dipeptidyl Peptidase 4 Inhibitor [EPC]
- Dipeptidyl Peptidase 4 Inhibitors [MoA]
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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.