SODIUM BICARBONATE
NDC 54738-020, SODIUM BICARBONATE, tablet, from Richmond Pharmaceuticals, Inc..
- Product NDC
- 54738-020
- Status
- Listed
- Labeler
- Richmond Pharmaceuticals, Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- OTC MONOGRAPH FINAL
- Application
- part331
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/54738-020 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM BICARBONATE650 mg/1
Pharmacologic classes
Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 54738-020-03 | 54738002003 | 1000 TABLET in 1 BOTTLE, PLASTIC (54738-020-03) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 54738-020 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/54738-020 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 54738-020. 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.