NDC 0615-1393

Divalproex sodium

Divalproex Sodium

Divalproex sodium is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Ncs Healthcare Of Ky, Inc Dba Vangard Labs. The primary component is Divalproex Sodium.

• Product ID: 0615-1393_0db335ac-0715-4471-a2e2-6d317d30ed5a
• NDC: 0615-1393
• Product Type: Human Prescription Drug
• Proprietary Name: Divalproex sodium
• Generic Name: Divalproex Sodium
• Dosage Form: Capsule
• Route of Administration: ORAL
• Marketing Start Date: 2009-01-23
• Marketing End Date: 2020-08-31
• Marketing Category: ANDA / ANDA
• Application Number: ANDA078979
• Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
• Substance Name: DIVALPROEX SODIUM
• Active Ingredient Strength: 125 mg/1
• Pharm Classes: Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC]
• NDC Exclude Flag: N

Packaging

NDC 0615-1393-05

15 CAPSULE in 1 BLISTER PACK (0615-1393-05)

• Marketing Start Date: 2009-01-23
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0615-1393-30 [00615139330]

Divalproex sodium CAPSULE

• Marketing Category: ANDA
• Application Number: ANDA078979
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2014-12-18
• Marketing End Date: 2020-07-31

NDC 0615-1393-39 [00615139339]

Divalproex sodium CAPSULE

• Marketing Category: ANDA
• Application Number: ANDA078979
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2010-01-25
• Marketing End Date: 2020-08-31

NDC 0615-1393-31 [00615139331]

Divalproex sodium CAPSULE

• Marketing Category: ANDA
• Application Number: ANDA078979
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2009-01-23
• Marketing End Date: 2016-03-14

NDC 0615-1393-05 [00615139305]

Divalproex sodium CAPSULE

• Marketing Category: ANDA
• Application Number: ANDA078979
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2010-01-25
• Marketing End Date: 2020-08-31

Drug Details

Active Ingredients

Ingredient	Strength
DIVALPROEX SODIUM	125 mg/1

OpenFDA Data

• SPL SET ID: 0a67fd2f-7fe8-4573-9be3-69ebe65a3ffe
• Manufacturer:
  • NCS HealthCare of KY, Inc dba Vangard Labs
• UNII:
  • 644VL95AO6
• RxNorm Concept Unique ID - RxCUI:
  • 1099596

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