Package 25021-797-05

Brand: valproate sodium

Generic: valproate sodium
NDC Package

Package Facts

Identity

Package NDC 25021-797-05
Digits Only 2502179705
Product NDC 25021-797
Product ID 25021-797_bac93779-c94f-49e9-90b7-5a53739b47be
Description

10 VIAL in 1 CARTON (25021-797-05) / 5 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2024-12-01
Brand valproate sodium
Generic valproate sodium
Sample Package No

Linked Drug Pages (1)

Valproate Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "bac93779-c94f-49e9-90b7-5a53739b47be", "openfda": {"unii": ["5VOM6GYJ0D"], "rxcui": ["1099648"], "spl_set_id": ["8d5fc1c1-d3c0-497e-971b-6c4dba9a3fad"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-797-05)  / 5 mL in 1 VIAL", "package_ndc": "25021-797-05", "marketing_start_date": "20241201"}], "brand_name": "Valproate Sodium", "product_id": "25021-797_bac93779-c94f-49e9-90b7-5a53739b47be", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "25021-797", "generic_name": "Valproate Sodium", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valproate Sodium", "active_ingredients": [{"name": "VALPROATE SODIUM", "strength": "100 mg/mL"}], "application_number": "ANDA076295", "marketing_category": "ANDA", "marketing_start_date": "20241201", "listing_expiration_date": "20261231"}