NDC product
TELMISARTAN and HYDROCHLOROTHIAZIDE
NDC 33342-130 · Macleods Pharmaceuticals Limited
Key facts
| Product NDC | 33342-130 |
|---|---|
| Proprietary name | TELMISARTAN and HYDROCHLOROTHIAZIDE |
| Labeler | Macleods Pharmaceuticals Limited |
| Marketing category | ANDA |
| Application number | ANDA204169 |
| Marketing start | Nov 2, 2015 |
| Marketing end | May 14, 2020 |
| Listing certified through | May 14, 2020 |
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: