NDC product
AMLODIPINE AND OLMESARTAN MEDOXOMIL
NDC 42571-237 · Micro Labs Limited
Key facts
| Product NDC | 42571-237 |
|---|---|
| Proprietary name | AMLODIPINE AND OLMESARTAN MEDOXOMIL |
| Nonproprietary name | Amlodipine and Olmesartan Medoxomil |
| Substances | AMLODIPINE BESYLATE, OLMESARTAN MEDOXOMIL |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | Micro Labs Limited |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA207435 |
| Pharmacologic classes | Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC] and 1 more |
| Marketing start | Jan 1, 2018 |
| 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: