Sodium Bicarbonate
- Product NDC
- 71872-7097
- 11-digit product format
- 718727097
- Labeler code
- 71872
- Product ID
- 71872-7097_fc5e6f2a-e811-0666-e053-6394a90a66a7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Bicarbonate
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 8MDF5V39QO | SODIUM BICARBONATE | 144-55-8 | SODIUM BICARBONATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7097-1 | 71872709701 | 1 CARTON in 1 BAG (71872-7097-1) / 1 SYRINGE in 1 CARTON / 50 mL in 1 SYRINGE | 1 carton | 2019-10-18 | No | No | Historical |