Sodium Bicarbonate
- Product NDC
- 69367-258
- 11-digit product format
- 693670258
- Labeler code
- 69367
- Product ID
- 69367-258_43b42880-bab8-4580-8a00-ae13855d44a3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Bicarbonate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Westminster Pharmaceuticals, LLC
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-10-10
- Substance
- SODIUM BICARBONATE
- Active strength
- 650 mg/1
- Pharmacologic classes
- Alkalinizing Activity [MoA]
- 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 |
|---|
| 69367-258-10 | Sodium Bicarbonate | 1000 in 1 BOTTLE | TABLET | 1000 | | 10 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69367-258 | SODIUM BICARBONATE TABLET [WESTMINSTER PHARMACEUTICALS, LLC] | 9 | Current NDC, Legacy NDC, 1 package rows | 20250425_9dcfc778-5fd6-4c68-8d37-a5385e374617.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 |
|---|
| 69367-258-10 | 69367025810 | 1000 TABLET in 1 BOTTLE (69367-258-10) | 1000 tablet | 2022-10-10 | 0000-00-00 | No | No | Current |