Sodium acetate anhydrous
- Product NDC
- 70069-048
- 11-digit product format
- 700690048
- Labeler code
- 70069
- Product ID
- 70069-048_1aae3237-9555-442b-b962-619d23f7e00a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium acetate anhydrous
- Dosage form
- SOLUTION, CONCENTRATE
- Route
- INTRAVENOUS
- Labeler
- Somerset Therapeutics, LLC
- Application
- ANDA219826
- Marketing category
- ANDA
- Marketing start
- 2025-10-23
- 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 anhydrous
- 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 |
|---|
| 70069-048-20 | Sodium acetate anhydrous | 20 in 1 CARTON | SOLUTION, CONCENTRATE | 20 | | 4 |
| 70069-048-20 | Sodium acetate anhydrous | 100 mL in 1 VIAL, GLASS | SOLUTION, CONCENTRATE | 100 | | 4 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 70069-048-20 | 70069004820 | 20 VIAL, GLASS in 1 CARTON (70069-048-20) / 100 mL in 1 VIAL, GLASS | 2025-10-23 | No | No | Current |