Package 55111-534-01

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 55111-534-01
Digits Only 5511153401
Product NDC 55111-534
Product ID 55111-534_0d557d96-7ebb-86b3-bdd1-af0b959bc845
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-534-01)

Marketing

Marketing Status
Marketed Since 2013-08-11
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": "0d557d96-7ebb-86b3-bdd1-af0b959bc845", "openfda": {"upc": ["0355111534013"], "unii": ["644VL95AO6"], "rxcui": ["1099569"], "spl_set_id": ["fa823ee0-0c69-6b85-da1e-9bb2e2150ea5"], "manufacturer_name": ["Dr. Reddy's Laboratories Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-534-01)", "package_ndc": "55111-534-01", "marketing_start_date": "20130811"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-534-05)", "package_ndc": "55111-534-05", "marketing_start_date": "20130811"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-534-30)", "package_ndc": "55111-534-30", "marketing_start_date": "20130811"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-534-60)", "package_ndc": "55111-534-60", "marketing_start_date": "20130811"}], "brand_name": "Divalproex Sodium", "product_id": "55111-534_0d557d96-7ebb-86b3-bdd1-af0b959bc845", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "55111-534", "generic_name": "Divalproex Sodium", "labeler_name": "Dr. Reddy's Laboratories Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA090070", "marketing_category": "ANDA", "marketing_start_date": "20130811", "listing_expiration_date": "20261231"}