Sodium Bicarbonate 10 gr. (650 mg)
- Product NDC
- 77333-829
- 11-digit product format
- 773330829
- Labeler code
- 77333
- Product ID
- 77333-829_4f52483b-6426-9646-e063-6394a90a5c0b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Bicarbonate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Gendose Pharmaceuticals, LLC
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-05-01
- Substance
- SODIUM BICARBONATE
- Active strength
- 650 mg/1
- Pharmacologic classes
- Alkalinizing Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sodium Bicarbonate 10 gr. (650 mg)
- Listing expiration
- 2027-12-31
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 |
|---|
| 77333-829-10 | Sodium Bicarbonate 10 gr. (650 mg) | 100 in 1 BOX, UNIT-DOSE | TABLET | 100 | | 1 |
| 77333-829-25 | Sodium Bicarbonate 10 gr. (650 mg) | 10 in 1 BLISTER PACK | TABLET | 10 | | 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 |
|---|
| 77333-829-10 | 77333082910 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (77333-829-10) / 10 TABLET in 1 BLISTER PACK (77333-829-25) | 100 blister pack | 2026-05-01 | No | No | Current |
| 77333-829-25 | 77333082925 | 10 in 1 BLISTER PACK | | | | | Historical |