NDC product
Atenolol and Chlorthalidone
NDC 70954-390 · ANI Pharmaceuticals, Inc.
Key facts
| Product NDC | 70954-390 |
|---|---|
| Proprietary name | Atenolol and Chlorthalidone |
| Nonproprietary name | Atenolol and Chlorthalidone |
| Substances | ATENOLOL, CHLORTHALIDONE |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | ANI Pharmaceuticals, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA215560 |
| Pharmacologic classes | Adrenergic beta-Antagonists [MoA], Increased Diuresis [PE], Thiazide-like Diuretic [EPC], beta-Adrenergic Blocker [EPC] |
| Marketing start | Oct 25, 2021 |
| 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: