NDC product
Acebutolol Hydrochloride
NDC 51407-667 · Golden State Medical Supply, Inc.
Key facts
| Product NDC | 51407-667 |
|---|---|
| Proprietary name | Acebutolol Hydrochloride |
| Nonproprietary name | Acebutolol Hydrochloride |
| Substances | ACEBUTOLOL HYDROCHLORIDE |
| Dosage form | CAPSULE |
| Route | ORAL |
| Labeler | Golden State Medical Supply, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA074007 |
| Pharmacologic classes | Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC] |
| Marketing start | Oct 18, 1995 |
| 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: