NDC 0591-5715

Amoxapine

Amoxapine

Amoxapine is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Actavis Pharma, Inc.. The primary component is Amoxapine.

• Product ID: 0591-5715_2271a75a-f4d1-4ed9-8d66-092721bcdb2e
• NDC: 0591-5715
• Product Type: Human Prescription Drug
• Proprietary Name: Amoxapine
• Generic Name: Amoxapine
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 1992-08-28
• Marketing Category: ANDA / ANDA
• Application Number: ANDA072691
• Labeler Name: Actavis Pharma, Inc.
• Substance Name: AMOXAPINE
• Active Ingredient Strength: 100 mg/1
• Pharm Classes: Tricyclic Antidepressant [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 0591-5715-01

100 TABLET in 1 BOTTLE, PLASTIC (0591-5715-01)

• Marketing Start Date: 1992-08-28
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0591-5715-01 [00591571501]

Amoxapine TABLET

• Marketing Category: ANDA
• Application Number: ANDA072691
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1992-08-28

Drug Details

Active Ingredients

Ingredient	Strength
AMOXAPINE	100 mg/1

OpenFDA Data

• SPL SET ID: a16297df-3158-48db-85e5-5cd506885556
• Manufacturer:
  • Actavis Pharma, Inc.
• UNII:
  • R63VQ857OT
• RxNorm Concept Unique ID - RxCUI:
  • 197364
  • 197365
  • 197366
  • 197363
• UPC Code:
  • 0305915715019

Pharmacological Class

• Tricyclic Antidepressant [EPC]
• Tricyclic Antidepressant [EPC]

NDC Crossover Matching brand name "Amoxapine" or generic name "Amoxapine"

NDC	Brand Name	Generic Name
0591-5713	Amoxapine	Amoxapine
0591-5714	Amoxapine	Amoxapine
0591-5715	Amoxapine	Amoxapine
0591-5716	Amoxapine	Amoxapine