Package 0143-9785-10
Brand: valproate sodium
Generic: valproate sodiumPackage Facts
Identity
Package NDC
0143-9785-10
Digits Only
0143978510
Product NDC
0143-9785
Description
10 VIAL, SINGLE-DOSE in 1 CARTON (0143-9785-10) / 5 mL in 1 VIAL, SINGLE-DOSE (0143-9785-01)
Marketing
Marketing Status
Brand
valproate sodium
Generic
valproate sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "0610e50d-6447-4a0e-bc36-dc0bffa95c7d", "openfda": {"unii": ["5VOM6GYJ0D"], "rxcui": ["1099648"], "spl_set_id": ["bcf57b31-4811-4104-82b3-46fb91a53ee0"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (0143-9785-10) / 5 mL in 1 VIAL, SINGLE-DOSE (0143-9785-01)", "package_ndc": "0143-9785-10", "marketing_start_date": "20100217"}], "brand_name": "Valproate Sodium", "product_id": "0143-9785_0610e50d-6447-4a0e-bc36-dc0bffa95c7d", "dosage_form": "INJECTION", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "0143-9785", "generic_name": "Valproate Sodium", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valproate Sodium", "active_ingredients": [{"name": "VALPROATE SODIUM", "strength": "500 mg/5mL"}], "application_number": "ANDA078523", "marketing_category": "ANDA", "marketing_start_date": "20100217", "listing_expiration_date": "20261231"}