Details for New Drug Application (NDA): 219701
The generic ingredient in SODIUM BICARBONATE is sodium bicarbonate. There is one drug master file entry for this compound. Twenty-three suppliers are listed for this compound. Additional details are available on the sodium bicarbonate profile page.
Summary for 219701
| Tradename: | SODIUM BICARBONATE |
| Applicant: | Adaptis |
| Ingredient: | sodium bicarbonate |
| Patents: | 0 |
Pharmacology for NDA: 219701
| Mechanism of Action | Alkalinizing Activity |
Suppliers and Packaging for NDA: 219701
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| SODIUM BICARBONATE | sodium bicarbonate | SOLUTION;INTRAVENOUS | 219701 | ANDA | Glenmark Pharmaceuticals Inc., USA | 68462-951 | 68462-951-65 | 25 VIAL in 1 CARTON (68462-951-65) / 50 mL in 1 VIAL (68462-951-50) |
| SODIUM BICARBONATE | sodium bicarbonate | SOLUTION;INTRAVENOUS | 219701 | ANDA | Medical Purchasing Solutions, LLC. | 71872-7376 | 71872-7376-1 | 1 VIAL in 1 BAG (71872-7376-1) / 50 mL in 1 VIAL |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;INTRAVENOUS | Strength | 50MEQ/50ML (1MEQ/ML) | ||||
| Approval Date: | Jun 26, 2025 | TE: | AP | RLD: | No | ||||
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