NDC 0832-7124

Divalproex Sodium

Divalproex Sodium

Divalproex Sodium is a Oral Tablet, Delayed Release in the Human Prescription Drug category. It is labeled and distributed by Upsher-smith Laboratories, Llc. The primary component is Divalproex Sodium.

• Product ID: 0832-7124_0103f7eb-58cb-45e9-bf7b-14e76fb86215
• NDC: 0832-7124
• Product Type: Human Prescription Drug
• Proprietary Name: Divalproex Sodium
• Generic Name: Divalproex Sodium
• Dosage Form: Tablet, Delayed Release
• Route of Administration: ORAL
• Marketing Start Date: 2014-03-21
• Marketing Category: ANDA / ANDA
• Application Number: ANDA078182
• Labeler Name: Upsher-Smith Laboratories, LLC
• Substance Name: DIVALPROEX SODIUM
• Active Ingredient Strength: 500 mg/1
• Pharm Classes: Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 0832-7124-01

100 BLISTER PACK in 1 CARTON (0832-7124-01) > 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0832-7124-89)

• Marketing Start Date: 2016-04-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0832-7124-15 [00832712415]

Divalproex Sodium TABLET, DELAYED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA078182
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2014-03-21

NDC 0832-7124-11 [00832712411]

Divalproex Sodium TABLET, DELAYED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA078182
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2014-03-21

NDC 0832-7124-89 [00832712489]

Divalproex Sodium TABLET, DELAYED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA078182
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2016-02-26

NDC 0832-7124-01 [00832712401]

Divalproex Sodium TABLET, DELAYED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA078182
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2016-04-01

Drug Details

Active Ingredients

Ingredient	Strength
DIVALPROEX SODIUM	500 mg/1

OpenFDA Data

• SPL SET ID: 02304a23-4a5f-47bc-9687-4044b43f7a20
• Manufacturer:
  • Upsher-Smith Laboratories, LLC
• UNII:
  • 644VL95AO6
• RxNorm Concept Unique ID - RxCUI:
  • 1099870
  • 1099625
  • 1099678
• UPC Code:
  • 0308327124110
  • 0308327122116

Pharmacological Class

• Anti-epileptic Agent [EPC]
• Decreased Central Nervous System Disorganized Electrical Activity [PE]
• Mood Stabilizer [EPC]

NDC Crossover Matching brand name "Divalproex Sodium" or generic name "Divalproex Sodium"

NDC	Brand Name	Generic Name
68001-105	Divalproex Sodium	Divalproex Sodium
68001-106	Divalproex Sodium	Divalproex Sodium
68071-4102	Divalproex Sodium	Divalproex Sodium
68084-313	divalproex sodium	divalproex sodium
68084-310	Divalproex Sodium	Divalproex Sodium
68084-415	Divalproex Sodium	Divalproex Sodium
68084-782	Divalproex Sodium	Divalproex Sodium
68084-776	Divalproex Sodium	Divalproex Sodium
68151-1164	Divalproex Sodium	Divalproex Sodium
68151-4162	Divalproex Sodium	Divalproex Sodium
68180-266	Divalproex Sodium	Divalproex Sodium
68180-267	Divalproex Sodium	Divalproex Sodium
68180-265	Divalproex Sodium	Divalproex Sodium
68382-032	Divalproex Sodium	Divalproex Sodium
68382-033	Divalproex Sodium	Divalproex Sodium
68382-031	Divalproex Sodium	Divalproex Sodium
68382-133	Divalproex Sodium	Divalproex Sodium
68382-134	Divalproex Sodium	Divalproex Sodium
68382-106	divalproex sodium	divalproex sodium
68788-7183	Divalproex Sodium	Divalproex Sodium
68788-7295	Divalproex Sodium	Divalproex Sodium
68788-7177	Divalproex sodium	Divalproex sodium
69189-0046	Divalproex Sodium	Divalproex Sodium
70518-0282	Divalproex Sodium	Divalproex Sodium
70518-0312	Divalproex Sodium	Divalproex Sodium
70518-0463	Divalproex Sodium	Divalproex Sodium
70518-0613	Divalproex Sodium	Divalproex Sodium
70518-0374	Divalproex Sodium	Divalproex Sodium
70518-1556	Divalproex Sodium	Divalproex Sodium
70518-1661	Divalproex Sodium	Divalproex Sodium
70518-1138	Divalproex Sodium	Divalproex Sodium
70518-1781	Divalproex sodium	Divalproex sodium
70518-1749	divalproex sodium	divalproex sodium
70518-1558	Divalproex Sodium	Divalproex Sodium
70518-1897	Divalproex sodium	Divalproex sodium
0615-1393	Divalproex sodium	Divalproex sodium
71335-0008	Divalproex Sodium	Divalproex Sodium
71610-205	Divalproex sodium	Divalproex sodium
71610-032	Divalproex Sodium	Divalproex Sodium
71610-157	Divalproex sodium	Divalproex sodium
71610-201	Divalproex Sodium	Divalproex Sodium
71610-030	Divalproex Sodium	Divalproex Sodium
0615-7532	Divalproex Sodium	Divalproex Sodium
0615-7531	Divalproex Sodium	Divalproex Sodium
0615-7533	Divalproex Sodium	Divalproex Sodium
0615-7554	Divalproex Sodium	Divalproex Sodium
71610-031	Divalproex Sodium	Divalproex Sodium
0615-7555	Divalproex Sodium	Divalproex Sodium
0615-7848	Divalproex Sodium	Divalproex Sodium
0615-7950	Divalproex Sodium	Divalproex Sodium