SODIUM ACETATE
- Product NDC
- 80830-2436
- 11-digit product format
- 808302436
- Labeler code
- 80830
- Product ID
- 80830-2436_023c3b27-6c16-438b-b43d-7f9f27ceea7f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sodium acetate
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- INTRAVENOUS
- Labeler
- Amneal Pharmaceuticals Private Limited
- Application
- ANDA218469
- Marketing category
- ANDA
- Marketing start
- 2025-08-12
- Substance
- SODIUM ACETATE ANHYDROUS
- Active strength
- 164 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- SODIUM ACETATE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM ACETATE ANHYDROUS | 164 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | NVG71ZZ7P0 |
| Rxcui | 237371 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 80830-2436-1 | SODIUM ACETATE | 50 mL in 1 VIAL, PHARMACY BULK PACKAGE | INJECTION, SOLUTION, CONCENTRATE | 50 | | 3 |
| 80830-2436-2 | SODIUM ACETATE | 25 in 1 CARTON | INJECTION, SOLUTION, CONCENTRATE | 25 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 80830-2436-1 | 80830243601 | 50 mL in 1 VIAL, PHARMACY BULK PACKAGE | 50 ml | | | | Historical |
| 80830-2436-2 | 80830243602 | 25 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (80830-2436-2) / 50 mL in 1 VIAL, PHARMACY BULK PACKAGE (80830-2436-1) | | 2025-08-12 | No | No | Current |