NDC 0074-6114

Depakote Sprinkles

Divalproex Sodium

Depakote Sprinkles is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Abbvie Inc.. The primary component is Divalproex Sodium.

• Product ID: 0074-6114_5214f621-667f-82d7-3cd3-f35163f72234
• NDC: 0074-6114
• Product Type: Human Prescription Drug
• Proprietary Name: Depakote Sprinkles
• Generic Name: Divalproex Sodium
• Dosage Form: Capsule
• Route of Administration: ORAL
• Marketing Start Date: 1989-09-12
• Marketing Category: NDA / NDA
• Application Number: NDA019680
• Labeler Name: AbbVie Inc.
• 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
• Listing Certified Through: 2020-12-31

Packaging

NDC 0074-6114-13

100 CAPSULE in 1 BOTTLE (0074-6114-13)

• Marketing Start Date: 1989-09-12
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0074-6114-11 [00074611411]

Depakote Sprinkles CAPSULE

• Marketing Category: NDA
• Application Number: NDA019680
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1989-09-12
• Marketing End Date: 2018-07-13

NDC 0074-6114-71 [00074611471]

Depakote Sprinkles CAPSULE

• Marketing Category: NDA
• Application Number: NDA019680
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2010-06-11
• Marketing End Date: 2013-08-14

NDC 0074-6114-13 [00074611413]

Depakote Sprinkles CAPSULE

• Marketing Category: NDA
• Application Number: NDA019680
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1989-09-12

Drug Details

Active Ingredients

Ingredient	Strength
DIVALPROEX SODIUM	125 mg/1

OpenFDA Data

• SPL SET ID: 4619aff4-0f80-444f-858d-42e4137aa809
• Manufacturer:
  • AbbVie Inc.
• UNII:
  • 644VL95AO6
• RxNorm Concept Unique ID - RxCUI:
  • 1099596
  • 1099598
• UPC Code:
  • 0300746114130

Pharmacological Class

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

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

NDC	Brand Name	Generic Name
0074-3826	Depakote	Divalproex Sodium
0074-6114	Depakote	Divalproex Sodium
0074-6212	Depakote	Divalproex Sodium
0074-6214	Depakote	Divalproex Sodium
0074-6215	Depakote	Divalproex Sodium
0074-7126	Depakote	Divalproex Sodium