Package 72189-010-30

Brand: valproic acid

Generic: valproic acid
NDC Package

Package Facts

Identity

Package NDC 72189-010-30
Digits Only 7218901030
Product NDC 72189-010
Description

30 CAPSULE in 1 BOTTLE (72189-010-30)

Marketing

Marketing Status
Marketed Since 2019-06-21
Brand valproic acid
Generic valproic acid
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c290b36-b0f4-2265-e063-6394a90af311", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751"], "unii": ["614OI1Z5WI"], "rxcui": ["1099681"], "spl_set_id": ["8bdbacb1-b38a-3282-e053-2a95a90af022"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]", "Mood Stabilizer [EPC]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (72189-010-30)", "package_ndc": "72189-010-30", "marketing_start_date": "20190621"}], "brand_name": "Valproic Acid", "product_id": "72189-010_2c290b36-b0f4-2265-e063-6394a90af311", "dosage_form": "CAPSULE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "72189-010", "generic_name": "Valproic Acid", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valproic Acid", "active_ingredients": [{"name": "VALPROIC ACID", "strength": "250 mg/1"}], "application_number": "ANDA073229", "marketing_category": "ANDA", "marketing_start_date": "20190621", "listing_expiration_date": "20261231"}