NDC product
Mefloquine Hydrochloride
NDC 62135-973 · Chartwell RX, LLC
Key facts
| Product NDC | 62135-973 |
|---|---|
| Proprietary name | Mefloquine Hydrochloride |
| Nonproprietary name | Mefloquine Hydrochloride |
| Substances | MEFLOQUINE HYDROCHLORIDE |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | Chartwell RX, LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA076175 |
| Pharmacologic classes | Antimalarial [EPC] |
| Marketing start | Feb 20, 2022 |
| Listing certified through | Dec 31, 2026 |
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: