Package 0074-6114-13

Brand: depakote sprinkles

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 0074-6114-13
Digits Only 0074611413
Product NDC 0074-6114
Product ID 0074-6114_b887d1d1-8485-47d1-bc35-7a80c31698b9
Description

100 CAPSULE in 1 BOTTLE (0074-6114-13)

Marketing

Marketing Status
Marketed Since 1989-09-12
Brand depakote sprinkles
Generic divalproex sodium
Sample Package No

Linked Drug Pages (1)

Depakote Sprinkles ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b887d1d1-8485-47d1-bc35-7a80c31698b9", "openfda": {"upc": ["0300746114130"], "unii": ["644VL95AO6"], "rxcui": ["1099596", "1099598"], "spl_set_id": ["4619aff4-0f80-444f-858d-42e4137aa809"], "manufacturer_name": ["AbbVie Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0074-6114-13)", "package_ndc": "0074-6114-13", "marketing_start_date": "19890912"}], "brand_name": "Depakote Sprinkles", "product_id": "0074-6114_b887d1d1-8485-47d1-bc35-7a80c31698b9", "dosage_form": "CAPSULE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "0074-6114", "generic_name": "Divalproex Sodium", "labeler_name": "AbbVie Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Depakote", "brand_name_suffix": "Sprinkles", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "125 mg/1"}], "application_number": "NDA019680", "marketing_category": "NDA", "marketing_start_date": "19890912", "listing_expiration_date": "20271231"}