Ingredient Name:
DIVALPROEX SODIUM
Ingredient ID:
644VL95AO6
Ingredient Code:
2.16.840.1.113883.6.1
Ing. ID Code System:
2.16.840.1.113883.4.9
Ingredient Short Description:
DIVALPROEX SODIUM is part of manufacturing ingredient used in FDA Database. When you consume you prescription drug make sure that you are not allergic to this DIVALPROEX SODIUM. This will change the way your body absorbs prescription drug your doctor provided you with. DIVALPROEX SODIUM is used in manufacturing process of pharmaceutical products. List bellow has DIVALPROEX SODIUM as ingredient during manufacturing.
As some Prescription Drugs might have same name but they are classified by FDA with uniq ID.
Ingredient DIVALPROEX SODIUM was found in these prescription drugs:
- DIVALPROEX SODIUM 3f4d8406-4049-0912-e054-00144ff8d46c (Class System:2.16.840.1.113883.6.1)
- DIVALPROEX SODIUM DELAYED-RELEASE TABLETS USP, 7439, 7440, 7441, Rx only e96fff12-7b42-4b58-8bd9-7b96eb2b120c (Class System:2.16.840.1.113883.6.1)
- DIVALPROEX SODIUM DELAYED-RELEASE TABLETS, USP 812b28bf-c62b-489e-8188-5901a3b23084 (Class System:2.16.840.1.113883.6.1)
- DIVALPROEX SODIUM DELAYED-RELEASE TABLETS c587a83e-6bd2-4645-8044-0884fbb2bc4f (Class System:2.16.840.1.113883.6.1)
- DIVALPROEX SODIUM 2228459e-b229-435d-99c7-793f86fb82e1 (Class System:2.16.840.1.113883.6.1)
- DIVALPROEX SODIUM 7cde8051-80fb-4f9e-b6f0-8780d19078e9 (Class System:2.16.840.1.113883.6.1)
- Divalproex Sodium Delayed Release Tablets USP 0a07f0df-9050-41bb-a892-f97fe0731ef7 (Class System:2.16.840.1.113883.6.1)
- DIVALPROEX SODIUM DELAYED-RELEASE TABLETS 714fe0a9-2eb5-49cd-bcb1-fda3f206331c (Class System:2.16.840.1.113883.6.1)