Sodium Bicarbonate
- Product NDC
- 84549-352
- 11-digit product format
- 845490352
- Labeler code
- 84549
- Product ID
- 84549-352_3d71b046-3e0c-054a-e063-6294a90a563a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Bicarbonate
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- ProPharma Distribution
- Application
- ANDA203449
- Marketing category
- ANDA
- Marketing start
- 2000-06-01
- 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 | 792582 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84549-352-01 | Sodium Bicarbonate | 50 mL in 1 SYRINGE | INJECTION | 50 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84549-352-01 | 84549035201 | 50 mL in 1 SYRINGE (84549-352-01) | 50 ml | 2025-09-01 | No | No | Historical |