Package 72189-459-60

Brand: divalproex sodium er

Generic: divalproex sodium er
NDC Package

Package Facts

Identity

Package NDC 72189-459-60
Digits Only 7218945960
Product NDC 72189-459
Product ID 72189-459_2c4dbb36-4841-f211-e063-6294a90ad364
Description

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-459-60)

Marketing

Marketing Status
Marketed Since 2023-04-03
Brand divalproex sodium er
Generic divalproex sodium er
Sample Package No

Linked Drug Pages (1)

Divalproex Sodium ER ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c4dbb36-4841-f211-e063-6294a90ad364", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099569"], "spl_set_id": ["f86f185b-4acb-43b5-e053-6394a90a681c"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-459-60)", "package_ndc": "72189-459-60", "marketing_start_date": "20230403"}], "brand_name": "Divalproex Sodium ER", "product_id": "72189-459_2c4dbb36-4841-f211-e063-6294a90ad364", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "72189-459", "generic_name": "Divalproex Sodium ER", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium ER", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA209286", "marketing_category": "ANDA", "marketing_start_date": "20230403", "listing_expiration_date": "20261231"}