Package 0641-6261-01

Brand: sodium acetate

Generic: sodium acetate
NDC Package

Package Facts

Identity

Package NDC 0641-6261-01
Digits Only 0641626101
Product NDC 0641-6261
Product ID 0641-6261_3493d4c1-4f73-44e8-94bc-7b55fe4fd436
Description

1 VIAL in 1 CARTON (0641-6261-01) / 20 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2024-05-20
Brand sodium acetate
Generic sodium acetate
Sample Package No

Linked Drug Pages (1)

Sodium Acetate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "3493d4c1-4f73-44e8-94bc-7b55fe4fd436", "openfda": {"unii": ["NVG71ZZ7P0"], "rxcui": ["1859490"], "spl_set_id": ["8a338072-6f1e-460c-b9ec-59cef4f3f597"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (0641-6261-01)  / 20 mL in 1 VIAL", "package_ndc": "0641-6261-01", "marketing_start_date": "20240520"}], "brand_name": "Sodium Acetate", "product_id": "0641-6261_3493d4c1-4f73-44e8-94bc-7b55fe4fd436", "dosage_form": "INJECTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "0641-6261", "generic_name": "Sodium Acetate", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Acetate", "active_ingredients": [{"name": "SODIUM ACETATE ANHYDROUS", "strength": "164 mg/mL"}], "application_number": "ANDA216920", "marketing_category": "ANDA", "marketing_start_date": "20240520", "listing_expiration_date": "20261231"}