Divalproex Sodium

Generic: Divalproex Sodium

Labeler: American Health Packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive

Drug Facts

Product Profile

Brand Name Divalproex Sodium
Generic Name Divalproex Sodium
Labeler American Health Packaging
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

DIVALPROEX SODIUM 125 mg/1

Identifiers & Regulatory

Product NDC 60687-211
Product ID 60687-211_2e2008f4-7e25-adb7-e063-6394a90a6a55
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090554
Marketing Start 2016-09-09
Marketing End 2026-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687211
Hyphenated Format 60687-211

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 Divalproex Sodium (source: ndc)
Generic Name Divalproex Sodium (source: ndc)
Application Number ANDA090554 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 125 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-211-21) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-211-11)
source: ndc

Packages (1)

60687-211-21 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-211-21) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-211-11)

Ingredients (1)

DIVALPROEX SODIUM (125 mg/1)

Linked Drug Pages (1)

Divalproex Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2e2008f4-7e25-adb7-e063-6394a90a6a55", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099625"], "spl_set_id": ["23dd3ef2-3ece-49ae-9133-f0ce10fd68fc"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-211-21)  / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-211-11)", "package_ndc": "60687-211-21", "marketing_end_date": "20260228", "marketing_start_date": "20160909"}], "brand_name": "Divalproex Sodium", "product_id": "60687-211_2e2008f4-7e25-adb7-e063-6394a90a6a55", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "60687-211", "generic_name": "Divalproex Sodium", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "125 mg/1"}], "application_number": "ANDA090554", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20160909"}