Divalproex sodium

CHEBI:CHEBI_746877

Drug Classification

Important Medical Information

⚕️ This information is sourced from ChEBI (Chemical Entities of Biological Interest) database and is intended for educational purposes only.

  • Always consult with a healthcare professional before starting, stopping, or modifying any medication.
  • Side effects may vary and this list may not be comprehensive.
  • Drug interactions may occur with other medications.

Additional Identifiers

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Additional Attributes

brand_name
Depakote ER
brand_name_base
divalproex sodium
generic_name
divalproex sodium
product_ndc
23639-0001
product_type
BULK INGREDIENT
marketing_category
BULK INGREDIENT
dosage_form
CAPSULE, COATED PELLETS
application_number
ANDA078790
route
ORAL
package_ndc
37662-0729-3
spl_id
df78479a-e481-1fc8-e053-2995a90a1ea6
listing_expiration_date
20241231
marketing_start_date
20090123
labeler_name
Anjan Drug Private Limited
package_marketing_start_date
12-SEP-89
package_description
120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-249-70)
manufacturer_name
NuCare Pharmceuticals,Inc.
pharm_class
Decreased Central Nervous System Disorganized Electrical Activity [PE]
active_ingredient_strength
1 [hp_M]/1
brand_name_suffix
Sprinkles
active_ingredient_name
VALPROATE SODIUM
upc
0055154714501
spl_set_id
4817535e-d9e9-4cc0-9212-e232cbd8c2fd
22-rdf-syntax-ns#type
http://www.w3.org/2002/07/owl#Class
rxcui
1099871
unii
5VOM6GYJ0D