Sodium Bicarbonate
- Product NDC
- 63629-8775
- 11-digit product format
- 636298775
- Labeler code
- 63629
- Product ID
- 63629-8775_72b60d17-e7fe-48d1-ad62-b5cca86c0296
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Bicarbonate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-07-20
- 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 |
|---|
| 63629-8775-1 | Sodium Bicarbonate | 1000 in 1 BOTTLE | TABLET | 1000 | | 104 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-8775 | SODIUM BICARBONATE TABLET [BRYANT RANCH PREPACK] | 104 | Current NDC, Legacy NDC, 1 package rows | 20240302_4493d7c5-f2c3-416e-a5c1-35398fc7f61d.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 |
|---|
| 63629-8775-1 | 63629877501 | 1000 TABLET in 1 BOTTLE (63629-8775-1) | 1000 tablet | 2021-08-17 | 0000-00-00 | No | No | Current |