Package 46708-821-31
Brand: divalproex sodium
Generic: divalproex sodiumPackage Facts
Identity
Package NDC
46708-821-31
Digits Only
4670882131
Product NDC
46708-821
Description
100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-821-31)
Marketing
Marketing Status
Brand
divalproex sodium
Generic
divalproex sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f34c4504-5409-406e-995b-138e5f700242", "openfda": {"upc": ["0346708821319"], "unii": ["644VL95AO6"], "rxcui": ["1099596"], "spl_set_id": ["f34c4504-5409-406e-995b-138e5f700242"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (46708-821-10) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "46708-821-10", "marketing_start_date": "20241223"}, {"sample": false, "description": "100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-821-31)", "package_ndc": "46708-821-31", "marketing_start_date": "20241223"}, {"sample": false, "description": "1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-821-91)", "package_ndc": "46708-821-91", "marketing_start_date": "20241223"}], "brand_name": "Divalproex sodium", "product_id": "46708-821_f34c4504-5409-406e-995b-138e5f700242", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "46708-821", "generic_name": "Divalproex sodium", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "125 mg/1"}], "application_number": "ANDA218793", "marketing_category": "ANDA", "marketing_start_date": "20241223", "listing_expiration_date": "20261231"}