Package 72603-260-01

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 72603-260-01
Digits Only 7260326001
Product NDC 72603-260
Product ID 72603-260_7306e665-f551-db56-f79a-624d7cd1225b
Description

100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72603-260-01)

Marketing

Marketing Status
Marketed Since 2024-08-01
Brand divalproex sodium
Generic divalproex sodium
Sample Package No

Linked Drug Pages (1)

Divalproex sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7306e665-f551-db56-f79a-624d7cd1225b", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099596"], "spl_set_id": ["589ae3a6-8b2e-d931-d36b-1937287ab5c0"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72603-260-01)", "package_ndc": "72603-260-01", "marketing_start_date": "20240801"}, {"sample": false, "description": "500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72603-260-02)", "package_ndc": "72603-260-02", "marketing_start_date": "20240801"}], "brand_name": "Divalproex sodium", "product_id": "72603-260_7306e665-f551-db56-f79a-624d7cd1225b", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "72603-260", "generic_name": "Divalproex sodium", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "125 mg/1"}], "application_number": "ANDA078979", "marketing_category": "ANDA", "marketing_start_date": "20240801", "listing_expiration_date": "20261231"}