Rapidol Sodium Bicarbonate
- Product NDC
- 55758-319
- 11-digit product format
- 557580319
- Labeler code
- 55758
- Product ID
- 55758-319_4df255cd-f223-1b0c-e063-6394a90ad6f7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Bicarbonate
- Dosage form
- POWDER
- Route
- ORAL
- Labeler
- Pharmadel LLC
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-11-23
- Substance
- SODIUM BICARBONATE
- Active strength
- 2.6 g/2.6g
- 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
- Rapidol Sodium Bicarbonate
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM BICARBONATE | 2.6 g/2.6g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8MDF5V39QO |
| Rxcui | 1488624 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 55758-319-04 | Rapidol Sodium Bicarbonate | 113 g in 1 BOTTLE | POWDER | 113 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55758-319 | RAPIDOL SODIUM BICARBONATE (SODIUM BICARBONATE) POWDER [PHARMADEL LLC] | 2 | Current NDC, 1 package rows | 20241120_b4c9a653-6f51-7c98-e053-2995a90ada37.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 55758-319-04 | 55758031904 | 113 g in 1 BOTTLE (55758-319-04) | 113 g | 2020-11-23 | No | No | Current |