Sodium Bicarbonate
- Product NDC
- 24689-137
- 11-digit product format
- 246890137
- Labeler code
- 24689
- Product ID
- 24689-137_08352100-b59d-c799-e063-6294a90a5e3b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Bicarbonate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- APNAR PHARMA LP
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-06-24
- 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 |
|---|
| 24689-137-01 | Sodium Bicarbonate | 1000 in 1 BOTTLE | TABLET | 1000 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 24689-137 | SODIUM BICARBONATE TABLET [APNAR PHARMA LP] | 4 | Current NDC, Legacy NDC, 1 package rows | 20231021_e206c240-55c2-2d00-e053-2a95a90a1779.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 |
|---|
| 24689-137-01 | 24689013701 | 1000 TABLET in 1 BOTTLE (24689-137-01) | 1000 tablet | 2022-06-24 | 0000-00-00 | No | No | Current |