SODIUM BICARBONATE
- Product NDC
- 51662-1400
- 11-digit product format
- 516621400
- Labeler code
- 51662
- Product ID
- 51662-1400_2b378e09-dfa6-64ea-e063-6294a90ab529
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SODIUM BICARBONATE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2019-10-19
- Substance
- SODIUM BICARBONATE
- Active strength
- 42 mg/mL
- 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 | 42 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8MDF5V39QO |
| Rxcui | 1868469 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51662-1400-1 | SODIUM BICARBONATE | 5 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SOLUTION | 5 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51662-1400 | SODIUM BICARBONATE INJECTION, SOLUTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST] | 3 | Current NDC, Legacy NDC, 1 package rows | 20250110_9545d58c-1c49-79b3-e053-2995a90a9d40.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 |
|---|
| 51662-1400-1 | 51662140001 | 5 mL in 1 VIAL, SINGLE-DOSE (51662-1400-1) | 5 ml | 2019-10-19 | 0000-00-00 | No | No | Current |