NDC product
Methenamine Hippurate
NDC 42571-332 · Micro Labs Limited
Key facts
| Product NDC | 42571-332 |
|---|---|
| Proprietary name | Methenamine Hippurate |
| Nonproprietary name | Methenamine Hippurate |
| Substances | METHENAMINE HIPPURATE |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | Micro Labs Limited |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA212172 |
| Marketing start | Aug 15, 2019 |
| 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: