Package 63323-494-16

Brand: valproate sodium

Generic: valproate sodium
NDC Package

Package Facts

Identity

Package NDC 63323-494-16
Digits Only 6332349416
Product NDC 63323-494
Product ID 63323-494_f09a2148-edd9-4918-8359-7554ed263d3a
Description

10 VIAL, SINGLE-DOSE in 1 TRAY (63323-494-16) / 5 mL in 1 VIAL, SINGLE-DOSE (63323-494-41)

Marketing

Marketing Status
Marketed Since 2003-08-18
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": "f09a2148-edd9-4918-8359-7554ed263d3a", "openfda": {"upc": ["0363323494414"], "unii": ["5VOM6GYJ0D"], "rxcui": ["1099648"], "spl_set_id": ["3dfb6da1-f66a-4618-9f74-d2d6c16c0b58"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 TRAY (63323-494-16)  / 5 mL in 1 VIAL, SINGLE-DOSE (63323-494-41)", "package_ndc": "63323-494-16", "marketing_start_date": "20030818"}], "brand_name": "Valproate Sodium", "product_id": "63323-494_f09a2148-edd9-4918-8359-7554ed263d3a", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "63323-494", "generic_name": "VALPROATE SODIUM", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valproate Sodium", "active_ingredients": [{"name": "VALPROATE SODIUM", "strength": "100 mg/mL"}], "application_number": "ANDA076539", "marketing_category": "ANDA", "marketing_start_date": "20030818", "listing_expiration_date": "20261231"}