Package 68084-782-61

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 68084-782-61
Digits Only 6808478261
Product NDC 68084-782
Product ID 68084-782_2e987eda-590b-fcc5-e063-6294a90aeb0d
Description

90 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-782-61) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (68084-782-11)

Marketing

Marketing Status
Discontinued 2026-06-30
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": "2e987eda-590b-fcc5-e063-6294a90aeb0d", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099678", "1099870"], "spl_set_id": ["64b509bc-f398-48ad-bdcb-9904e61d9225"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "90 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-782-61)  / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (68084-782-11)", "package_ndc": "68084-782-61", "marketing_end_date": "20260630", "marketing_start_date": "20160126"}], "brand_name": "Divalproex Sodium", "product_id": "68084-782_2e987eda-590b-fcc5-e063-6294a90aeb0d", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "68084-782", "generic_name": "Divalproex Sodium", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA090554", "marketing_category": "ANDA", "marketing_start_date": "20160126", "listing_expiration_date": "20261231"}