NDC product
tamsulosin hydrochloride
NDC 0781-2076 · Sandoz Inc
Key facts
| Product NDC | 0781-2076 |
|---|---|
| Proprietary name | tamsulosin hydrochloride |
| Nonproprietary name | tamsulosin hydrochloride |
| Substances | TAMSULOSIN HYDROCHLORIDE |
| Dosage form | CAPSULE |
| Route | ORAL |
| Labeler | Sandoz Inc |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA078015 |
| Pharmacologic classes | Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC] |
| Marketing start | Apr 27, 2010 |
| 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: