SODIUM BICARBONATE
- Product NDC
- 84549-050
- 11-digit product format
- 845490050
- Labeler code
- 84549
- Product ID
- 84549-050_463cedaa-4d0f-c9b6-e063-6394a90a8b31
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SODIUM BICARBONATE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- ProPharma Distribution
- Application
- ANDA217594
- Marketing category
- ANDA
- Marketing start
- 2024-03-15
- Substance
- SODIUM BICARBONATE
- Active strength
- 84 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 | 84 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8MDF5V39QO |
| Rxcui | 1868486 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84549-050-03 | SODIUM BICARBONATE | 50 mL in 1 VIAL | INJECTION, SOLUTION | 50 | | 4 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84549-050-03 | 84549005003 | 50 mL in 1 VIAL (84549-050-03) | 50 ml | 2025-08-27 | No | No | Historical |