Package 71335-1883-2
Brand: divalproex sodium
Generic: divalproex sodiumPackage Facts
Identity
Package NDC
71335-1883-2
Digits Only
7133518832
Product NDC
71335-1883
Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1883-2)
Marketing
Marketing Status
Brand
divalproex sodium
Generic
divalproex sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6dcd8d8d-3860-46c8-a8dd-3003604bc821", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099569"], "spl_set_id": ["0822300b-68c0-4e70-b1ba-8eb42cf373f7"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1883-1)", "package_ndc": "71335-1883-1", "marketing_start_date": "20240718"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1883-2)", "package_ndc": "71335-1883-2", "marketing_start_date": "20210621"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1883-3)", "package_ndc": "71335-1883-3", "marketing_start_date": "20220818"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1883-4)", "package_ndc": "71335-1883-4", "marketing_start_date": "20220818"}], "brand_name": "Divalproex sodium", "product_id": "71335-1883_6dcd8d8d-3860-46c8-a8dd-3003604bc821", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "71335-1883", "generic_name": "Divalproex sodium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA209286", "marketing_category": "ANDA", "marketing_start_date": "20200918", "listing_expiration_date": "20261231"}