Sodium Bicarbonate
- Product NDC
- 10135-684
- 11-digit product format
- 101350684
- Labeler code
- 10135
- Product ID
- 10135-684_8cebbe6f-e18b-4d3e-8512-8b2e61fc036b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Bicarbonate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Marlex Pharmaceuticals Inc
- Application
- part334
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-03-01
- Marketing end
- 0000-00-00
- Substance
- SODIUM BICARBONATE
- Active strength
- 325 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10135-684-10 | Sodium Bicarbonate | 1000 in 1 BOTTLE | TABLET | 1000 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10135-684 | SODIUM BICARBONATE TABLET [MARLEX PHARMACEUTICALS INC] | 2 | Legacy NDC, 1 package rows | 20211209_36c01ccb-1129-4e7f-9014-86f6ec1c14de.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 |
|---|
| 10135-684-10 | 10135068410 | 1000 TABLET in 1 BOTTLE (10135-684-10) | 1000 tablet | 2020-03-01 | 0000-00-00 | No | No | Current |