Package 63187-742-60

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 63187-742-60
Digits Only 6318774260
Product NDC 63187-742
Description

60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-742-60)

Marketing

Marketing Status
Marketed Since 2016-10-03
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": "ea6ad932-2a45-4117-9f1d-b21d2b0a1905", "openfda": {"upc": ["0363187742300", "0363187743901"], "unii": ["644VL95AO6"], "rxcui": ["1099678", "1099870"], "spl_set_id": ["abac11e6-7ce1-491c-9ac3-61f3df54c4a4"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-742-30)", "package_ndc": "63187-742-30", "marketing_start_date": "20161003"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-742-60)", "package_ndc": "63187-742-60", "marketing_start_date": "20161003"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-742-90)", "package_ndc": "63187-742-90", "marketing_start_date": "20161003"}], "brand_name": "Divalproex Sodium", "product_id": "63187-742_ea6ad932-2a45-4117-9f1d-b21d2b0a1905", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "63187-742", "generic_name": "Divalproex Sodium", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA079163", "marketing_category": "ANDA", "marketing_start_date": "20111001", "listing_expiration_date": "20261231"}