FDA NDC Directory · JSON-LD · Markdown
NDC 64764-335 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED
| Generic name | alogliptin and metformin hydrochloride |
|---|---|
| Labeler / Manufacturer | Takeda Pharmaceuticals America, Inc. |
| Marketing category | New Drug Application (innovator) · App NDA203414 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | ALOGLIPTIN BENZOATE (12.5 mg/1) METFORMIN HYDROCHLORIDE (500 mg/1) |
| Marketing started | 20130125 |
| Package count | 4 |
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