SODIUM BICARBONATE
NDC 70095-050, SODIUM BICARBONATE, injection, solution, from Sun Pharmaceutical Industries, Inc..
- Product NDC
- 70095-050
- Status
- Listed
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA217594
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70095-050 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM BICARBONATE84 mg/mL
Pharmacologic classes
Alkalinizing Activity [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70095-050-03 | 70095005003 | 25 VIAL in 1 CARTON (70095-050-03) / 50 mL in 1 VIAL (70095-050-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/5ae65432-04a1-4b6b-8536-2535064fc782NADAC price for package 70095005003
GET /v1/drugs/nadac/70095005003
Use it
Look up 70095-050 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70095-050 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70095-050. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.