Package 70069-048-20

Brand: sodium acetate anhydrous

Generic: sodium acetate anhydrous
NDC Package

Package Facts

Identity

Package NDC 70069-048-20
Digits Only 7006904820
Product NDC 70069-048
Product ID 70069-048_1aae3237-9555-442b-b962-619d23f7e00a
Description

20 VIAL, GLASS in 1 CARTON (70069-048-20) / 100 mL in 1 VIAL, GLASS

Marketing

Marketing Status
Marketed Since 2025-10-23
Brand sodium acetate anhydrous
Generic sodium acetate anhydrous
Sample Package No

Linked Drug Pages (1)

Sodium acetate anhydrous ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "1aae3237-9555-442b-b962-619d23f7e00a", "openfda": {"upc": ["0370069047255", "0370069048207", "0370069047019", "0370069048016"], "unii": ["NVG71ZZ7P0"], "rxcui": ["237371"], "spl_set_id": ["93edebd6-ef7f-483a-80b6-bfaf34ea5ded"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 VIAL, GLASS in 1 CARTON (70069-048-20)  / 100 mL in 1 VIAL, GLASS", "package_ndc": "70069-048-20", "marketing_start_date": "20251023"}], "brand_name": "Sodium acetate anhydrous", "product_id": "70069-048_1aae3237-9555-442b-b962-619d23f7e00a", "dosage_form": "SOLUTION, CONCENTRATE", "product_ndc": "70069-048", "generic_name": "Sodium acetate anhydrous", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium acetate anhydrous", "active_ingredients": [{"name": "SODIUM ACETATE ANHYDROUS", "strength": "164 mg/mL"}], "application_number": "ANDA219826", "marketing_category": "ANDA", "marketing_start_date": "20251023", "listing_expiration_date": "20261231"}