Package 72789-354-01

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 72789-354-01
Digits Only 7278935401
Product NDC 72789-354
Product ID 72789-354_4bbf5b62-d603-660c-e063-6294a90a73bb
Description

100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-354-01)

Marketing

Marketing Status
Marketed Since 2023-10-17
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": "4bbf5b62-d603-660c-e063-6294a90a73bb", "openfda": {"upc": ["0372789354019"], "unii": ["644VL95AO6"], "rxcui": ["1099870"], "spl_set_id": ["a67855ff-a879-43f0-bca3-94c304348bf5"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-354-01)", "package_ndc": "72789-354-01", "marketing_start_date": "20231017"}], "brand_name": "Divalproex Sodium", "product_id": "72789-354_4bbf5b62-d603-660c-e063-6294a90a73bb", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "72789-354", "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": "500 mg/1"}], "application_number": "ANDA078597", "marketing_category": "ANDA", "marketing_start_date": "20080729", "listing_expiration_date": "20271231"}