Package 71335-2124-1
Brand: divalproex sodium
Generic: divalproex sodiumPackage Facts
Identity
Package NDC
71335-2124-1
Digits Only
7133521241
Product NDC
71335-2124
Description
60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71335-2124-1)
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": "f10370ba-de96-42ac-bba9-e29400129dc7", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099870"], "spl_set_id": ["79e6dc26-a38b-4642-a216-1fa1213b919a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71335-2124-1)", "package_ndc": "71335-2124-1", "marketing_start_date": "20220719"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71335-2124-2)", "package_ndc": "71335-2124-2", "marketing_start_date": "20220719"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71335-2124-3)", "package_ndc": "71335-2124-3", "marketing_start_date": "20220719"}, {"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71335-2124-4)", "package_ndc": "71335-2124-4", "marketing_start_date": "20220719"}], "brand_name": "Divalproex Sodium", "product_id": "71335-2124_f10370ba-de96-42ac-bba9-e29400129dc7", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "71335-2124", "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": "ANDA079163", "marketing_category": "ANDA", "marketing_start_date": "20111001", "listing_expiration_date": "20261231"}