Package 0378-0473-05

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 0378-0473-05
Digits Only 0378047305
Product NDC 0378-0473
Product ID 0378-0473_1d6676f1-24a8-44aa-aa49-1a81c0705436
Description

500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-0473-05)

Marketing

Marketing Status
Marketed Since 2009-02-02
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": "1d6676f1-24a8-44aa-aa49-1a81c0705436", "openfda": {"upc": ["0303780473010", "0303780472013"], "unii": ["644VL95AO6"], "rxcui": ["1099563", "1099569"], "spl_set_id": ["00332c65-edad-a153-9c78-628931daa732"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-0473-01)", "package_ndc": "0378-0473-01", "marketing_start_date": "20090202"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-0473-05)", "package_ndc": "0378-0473-05", "marketing_start_date": "20090202"}], "brand_name": "Divalproex Sodium", "product_id": "0378-0473_1d6676f1-24a8-44aa-aa49-1a81c0705436", "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": "0378-0473", "generic_name": "divalproex sodium", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA077567", "marketing_category": "ANDA", "marketing_start_date": "20090202", "listing_expiration_date": "20271231"}