Package 71335-2862-1

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 71335-2862-1
Digits Only 7133528621
Product NDC 71335-2862
Product ID 71335-2862_41d88ff2-2260-8447-e063-6294a90aea0e
Description

100 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2862-1)

Marketing

Marketing Status
Marketed Since 2025-10-23
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": "41d88ff2-2260-8447-e063-6294a90aea0e", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099678"], "spl_set_id": ["1107f190-bef1-41cb-9393-8479b0a56040"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2862-1)", "package_ndc": "71335-2862-1", "marketing_start_date": "20251023"}], "brand_name": "Divalproex Sodium", "product_id": "71335-2862_41d88ff2-2260-8447-e063-6294a90aea0e", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "71335-2862", "generic_name": "Divalproex Sodium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA079163", "marketing_category": "ANDA", "marketing_start_date": "20111001", "listing_expiration_date": "20261231"}