NDC product
SODIUM BICARBONATE
NDC 70095-050 · Sun Pharmaceutical Industries Limited
Key facts
| Product NDC | 70095-050 |
|---|---|
| Proprietary name | SODIUM BICARBONATE |
| Nonproprietary name | SODIUM BICARBONATE |
| Substances | SODIUM BICARBONATE |
| Dosage form | INJECTION, SOLUTION |
| Route | INTRAVENOUS |
| Labeler | Sun Pharmaceutical Industries Limited |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA217594 |
| Pharmacologic classes | Alkalinizing Activity [MoA] |
| Marketing start | Mar 15, 2024 |
| 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: