Package 60687-868-01

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 60687-868-01
Digits Only 6068786801
Product NDC 60687-868
Product ID 60687-868_3a9c13b7-690a-9438-e063-6394a90ac202
Description

100 BLISTER PACK in 1 CARTON (60687-868-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-868-11)

Marketing

Marketing Status
Marketed Since 2025-03-21
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": "3a9c13b7-690a-9438-e063-6394a90ac202", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099625", "1099678", "1099870"], "spl_set_id": ["ca6bbec6-5631-4436-957e-fb8707e1683d"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-868-01)  / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-868-11)", "package_ndc": "60687-868-01", "marketing_start_date": "20250321"}], "brand_name": "Divalproex Sodium", "product_id": "60687-868_3a9c13b7-690a-9438-e063-6394a90ac202", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "60687-868", "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": "250 mg/1"}], "application_number": "ANDA079163", "marketing_category": "ANDA", "marketing_start_date": "20250321", "listing_expiration_date": "20261231"}