Package 0641-6263-10
Brand: sodium acetate
Generic: sodium acetatePackage Facts
Identity
Package NDC
0641-6263-10
Digits Only
0641626310
Product NDC
0641-6263
Description
10 VIAL in 1 CARTON (0641-6263-10) / 100 mL in 1 VIAL (0641-6263-01)
Marketing
Marketing Status
Brand
sodium acetate
Generic
sodium acetate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "777b7564-f07b-401a-a042-0cd512ae3b25", "openfda": {"unii": ["NVG71ZZ7P0"], "rxcui": ["237371"], "spl_set_id": ["7ee23a1c-bc99-4ff6-b2e7-d2aa42744553"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (0641-6263-10) / 100 mL in 1 VIAL (0641-6263-01)", "package_ndc": "0641-6263-10", "marketing_start_date": "20240520"}], "brand_name": "Sodium Acetate", "product_id": "0641-6263_777b7564-f07b-401a-a042-0cd512ae3b25", "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": "0641-6263", "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"}