NDC 0615-7555

Divalproex Sodium

Divalproex Sodium

Divalproex Sodium is a Oral Tablet, Film Coated, Extended Release 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: 0615-7555_5d008b40-c3a8-48e1-8b9a-142590e1a287
• NDC: 0615-7555
• Product Type: Human Prescription Drug
• Proprietary Name: Divalproex Sodium
• Generic Name: Divalproex Sodium
• Dosage Form: Tablet, Film Coated, Extended Release
• Route of Administration: ORAL
• Marketing Start Date: 2002-02-28
• Marketing End Date: 2020-08-31
• Marketing Category: ANDA / ANDA
• Application Number: ANDA077567
• Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
• 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

Packaging

NDC 0615-7555-39

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-7555-39)

• Marketing Start Date: 2010-02-08
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0615-7555-30 [00615755530]

Divalproex Sodium TABLET, FILM COATED, EXTENDED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA077567
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2015-01-27
• Marketing End Date: 2020-06-30

NDC 0615-7555-05 [00615755505]

Divalproex Sodium TABLET, FILM COATED, EXTENDED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA077567
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2009-09-30
• Marketing End Date: 2020-08-31

NDC 0615-7555-39 [00615755539]

Divalproex Sodium TABLET, FILM COATED, EXTENDED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA077567
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2009-09-30
• Marketing End Date: 2020-08-31

Drug Details

Active Ingredients

Ingredient	Strength
DIVALPROEX SODIUM	500 mg/1

OpenFDA Data

• SPL SET ID: e2015ac5-0441-43fd-b864-a1b1fe944450
• Manufacturer:
  • NCS HealthCare of KY, Inc dba Vangard Labs
• UNII:
  • 644VL95AO6
• RxNorm Concept Unique ID - RxCUI:
  • 1099563
  • 1099569

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