Sodium Bicarbonate
- Product NDC
- 80513-611
- 11-digit product format
- 805130611
- Labeler code
- 80513
- Product ID
- 80513-611_3d912fde-5c7a-e74c-e063-6394a90a6e1f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Bicarbonate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Advanced Rx LLC
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-09-01
- 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
- Brand name suffix
- 10 GR (650 MG)
- 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 |
|---|
| 80513-611-02 | Sodium Bicarbonate10 GR (650 MG) | 200 in 1 BOTTLE | TABLET | 200 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 80513-611-02 | 80513061102 | 200 TABLET in 1 BOTTLE (80513-611-02) | 200 tablet | 2025-09-01 | No | No | Current |