Package 60687-211-21

Brand: Divalproex Sodium

Generic: Divalproex Sodium
NDC Package

Package Facts

Identity

Package NDC 60687-211-21
Digits Only 6068721121
Product NDC 60687-211
Product ID 60687-211_2e2008f4-7e25-adb7-e063-6394a90a6a55
Description

30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-211-21) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-211-11)

Marketing

Marketing Status
Discontinued 2026-02-28
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": "2e2008f4-7e25-adb7-e063-6394a90a6a55", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099625"], "spl_set_id": ["23dd3ef2-3ece-49ae-9133-f0ce10fd68fc"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-211-21)  / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-211-11)", "package_ndc": "60687-211-21", "marketing_end_date": "20260228", "marketing_start_date": "20160909"}], "brand_name": "Divalproex Sodium", "product_id": "60687-211_2e2008f4-7e25-adb7-e063-6394a90a6a55", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "60687-211", "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": "125 mg/1"}], "application_number": "ANDA090554", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20160909"}