NDC product
MECLIZINE HYDROCHLORIDE
NDC 59651-809 · Aurobindo Pharma Limited
Key facts
| Product NDC | 59651-809 |
|---|---|
| Proprietary name | MECLIZINE HYDROCHLORIDE |
| Nonproprietary name | MECLIZINE |
| Substances | MECLIZINE HYDROCHLORIDE |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | Aurobindo Pharma Limited |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA202640 |
| Pharmacologic classes | Antiemetic [EPC], Emesis Suppression [PE] |
| Marketing start | Sep 14, 2023 |
| 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: