Package 72789-286-60
Brand: divalproex sodium
Generic: divalproex sodiumPackage Facts
Identity
Package NDC
72789-286-60
Digits Only
7278928660
Product NDC
72789-286
Description
60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-286-60)
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": "3caae1a2-be5d-809c-e063-6294a90ad105", "openfda": {"upc": ["0372789286600"], "unii": ["644VL95AO6"], "rxcui": ["1099563"], "spl_set_id": ["392df14f-4d65-4be9-973b-1f0ce1013d8f"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-286-60)", "package_ndc": "72789-286-60", "marketing_start_date": "20221117"}], "brand_name": "Divalproex sodium", "product_id": "72789-286_3caae1a2-be5d-809c-e063-6294a90ad105", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "72789-286", "generic_name": "Divalproex sodium", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA209286", "marketing_category": "ANDA", "marketing_start_date": "20200918", "listing_expiration_date": "20261231"}