depakote sprinkles

Generic: divalproex sodium

Labeler: abbvie inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name depakote sprinkles
Generic Name divalproex sodium
Labeler abbvie inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

divalproex sodium 125 mg/1

Manufacturer
AbbVie Inc.

Identifiers & Regulatory

Product NDC 0074-6114
Product ID 0074-6114_b887d1d1-8485-47d1-bc35-7a80c31698b9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019680
Listing Expiration 2027-12-31
Marketing Start 1989-09-12

Pharmacologic Class

Classes
anti-epileptic agent [epc] decreased central nervous system disorganized electrical activity [pe] mood stabilizer [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00746114
Hyphenated Format 0074-6114

Supplemental Identifiers

RxCUI
1099596 1099598
UPC
0300746114130
UNII
644VL95AO6

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name depakote sprinkles (source: ndc)
Generic Name divalproex sodium (source: ndc)
Application Number NDA019680 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 125 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (0074-6114-13)
source: ndc

Packages (1)

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

Ingredients (1)

divalproex sodium (125 mg/1)

Linked Drug Pages (1)

Depakote Sprinkles ndc-match (0.9)

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"}