divalproex sodium

Generic: divalproex sodium

Labeler: dr.reddy's laboratories limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name divalproex sodium
Generic Name divalproex sodium
Labeler dr.reddy's laboratories limited
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

divalproex sodium 500 mg/1

Manufacturer
Dr.Reddy's Laboratories Limited

Identifiers & Regulatory

Product NDC 55111-531
Product ID 55111-531_be502229-0e61-8481-dda9-794c93637dd7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078755
Listing Expiration 2026-12-31
Marketing Start 2008-07-29

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 55111531
Hyphenated Format 55111-531

Supplemental Identifiers

RxCUI
1099625 1099678 1099870
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 divalproex sodium (source: ndc)
Generic Name divalproex sodium (source: ndc)
Application Number ANDA078755 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-531-01)
  • 500 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-531-05)
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-531-30)
  • 10 BLISTER PACK in 1 CARTON (55111-531-78) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-531-79)
source: ndc

Packages (4)

55111-531-01 100 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-531-01) 55111-531-05 500 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-531-05) 55111-531-30 30 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-531-30) 55111-531-78 10 BLISTER PACK in 1 CARTON (55111-531-78) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-531-79)

Ingredients (1)

divalproex sodium (500 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": "be502229-0e61-8481-dda9-794c93637dd7", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099625", "1099678", "1099870"], "spl_set_id": ["15f8a5be-e269-2e07-60d9-1dd7bf5f5281"], "manufacturer_name": ["Dr.Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-531-01)", "package_ndc": "55111-531-01", "marketing_start_date": "20080729"}, {"sample": false, "description": "500 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-531-05)", "package_ndc": "55111-531-05", "marketing_start_date": "20080729"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-531-30)", "package_ndc": "55111-531-30", "marketing_start_date": "20080729"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (55111-531-78)  / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-531-79)", "package_ndc": "55111-531-78", "marketing_start_date": "20080729"}], "brand_name": "divalproex sodium", "product_id": "55111-531_be502229-0e61-8481-dda9-794c93637dd7", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "55111-531", "generic_name": "divalproex sodium", "labeler_name": "Dr.Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "divalproex sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA078755", "marketing_category": "ANDA", "marketing_start_date": "20080729", "listing_expiration_date": "20261231"}