NDC product
Pioglitazone Hydrochloride and Metformin Hydrochloride
NDC 57237-218 · Rising Pharma Holdings, Inc.
Key facts
| Product NDC | 57237-218 |
|---|---|
| Proprietary name | Pioglitazone Hydrochloride and Metformin Hydrochloride |
| Nonproprietary name | Pioglitazone Hydrochloride and Metformin Hydrochloride |
| Substances | PIOGLITAZONE HYDROCHLORIDE, METFORMIN HYDROCHLORIDE |
| Dosage form | TABLET, FILM COATED |
| Route | ORAL |
| Labeler | Rising Pharma Holdings, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA200823 |
| Pharmacologic classes | Biguanide [EPC], Biguanides [CS], Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator Receptor gamma Agonist [EPC], Peroxisome Proliferator-activated Receptor alpha Agonists [MoA], Peroxisome Proliferator-activated Receptor gamma Agonists [MoA] and 2 more |
| Marketing start | Feb 13, 2013 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: