SODIUM BICARBONATE
- Product NDC
- 54738-020
- 11-digit product format
- 547380020
- Labeler code
- 54738
- Product ID
- 54738-020_5cc6cec2-9f03-6cf9-e053-2991aa0ada77
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM BICARBONATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Richmond Pharmaceuticals, Inc.
- Application
- part331
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2015-05-01
- Substance
- SODIUM BICARBONATE
- Active strength
- 650 mg/1
- Pharmacologic classes
- Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- SODIUM BICARBONATE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM BICARBONATE | 650 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8MDF5V39QO |
| Rxcui | 198861 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 54738-020-03 | SODIUM BICARBONATE | 1000 in 1 BOTTLE, PLASTIC | TABLET | 1000 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 54738-020 | SODIUM BICARBONATE TABLET [RICHMOND PHARMACEUTICALS, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20171030_fa10d93d-b3ed-4675-a117-f573d9e72bca.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 54738-020-03 | 54738002003 | 1000 TABLET in 1 BOTTLE, PLASTIC (54738-020-03) | 1000 tablet | 2015-05-01 | 0000-00-00 | No | No | Current |