NDC product
Procainamide Hydrochloride
NDC 65145-155 · Caplin Steriles Limited
Key facts
| Product NDC | 65145-155 |
|---|---|
| Proprietary name | Procainamide Hydrochloride |
| Nonproprietary name | Procainamide Hydrochloride |
| Substances | PROCAINAMIDE HYDROCHLORIDE |
| Dosage form | INJECTION, SOLUTION |
| Route | INTRAMUSCULAR, INTRAVENOUS |
| Labeler | Caplin Steriles Limited |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA218674 |
| Pharmacologic classes | Antiarrhythmic [EPC] |
| Marketing start | Feb 17, 2025 |
| 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: