Package 71610-157-75

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 71610-157-75
Digits Only 7161015775
Product NDC 71610-157
Product ID 71610-157_33511714-8ded-46ee-ae1d-03a536728d31
Description

150 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-157-75)

Marketing

Marketing Status
Marketed Since 2018-09-20
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": "33511714-8ded-46ee-ae1d-03a536728d31", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099563"], "spl_set_id": ["ad5e8bd8-c923-40f0-a106-55620c4247d7"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-157-60)", "package_ndc": "71610-157-60", "marketing_start_date": "20180920"}, {"sample": false, "description": "150 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-157-75)", "package_ndc": "71610-157-75", "marketing_start_date": "20180920"}], "brand_name": "Divalproex sodium", "product_id": "71610-157_33511714-8ded-46ee-ae1d-03a536728d31", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "71610-157", "generic_name": "Divalproex sodium", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA202419", "marketing_category": "ANDA", "marketing_start_date": "20140602", "listing_expiration_date": "20261231"}