NDC 68382-133

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 Zydus Pharmaceuticals (usa) Inc.. The primary component is Divalproex Sodium.

• Product ID: 68382-133_0807c44b-85a7-4fc6-ad3d-f0985c640e02
• NDC: 68382-133
• 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: 2013-01-07
• Marketing Category: ANDA / ANDA
• Application Number: ANDA078239
• Labeler Name: Zydus Pharmaceuticals (USA) Inc.
• Substance Name: DIVALPROEX SODIUM
• Active Ingredient Strength: 250 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: 2021-12-31

Packaging

NDC 68382-133-01

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-133-01)

• Marketing Start Date: 2013-01-07
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68382-133-01 [68382013301]

Divalproex Sodium TABLET, FILM COATED, EXTENDED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA078239
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2013-01-07

NDC 68382-133-14 [68382013314]

Divalproex Sodium TABLET, FILM COATED, EXTENDED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA078239
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2013-01-07

NDC 68382-133-05 [68382013305]

Divalproex Sodium TABLET, FILM COATED, EXTENDED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA078239
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2013-01-07

NDC 68382-133-16 [68382013316]

Divalproex Sodium TABLET, FILM COATED, EXTENDED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA078239
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2013-01-07

Drug Details

Active Ingredients

Ingredient	Strength
DIVALPROEX SODIUM	250 mg/1

OpenFDA Data

• SPL SET ID: 2477f209-5853-4ac1-982d-b23aeb1c5d0c
• Manufacturer:
  • Zydus Pharmaceuticals (USA) Inc.
• UNII:
  • 644VL95AO6
• RxNorm Concept Unique ID - RxCUI:
  • 1099563
  • 1099569
• UPC Code:
  • 0368382134011
  • 0368382133014

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