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NDC 70934-0071-30 AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 Details

AMITRIPTYLINE HYDROCHLORIDE 25 mg/1

AMITRIPTYLINE HYDROCHLORIDE is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is AMITRIPTYLINE HYDROCHLORIDE.

MedlinePlus Drug Summary

Amitriptyline is used to treat symptoms of depression. Amitriptyline is in a class of medications called tricyclic antidepressants. It works by increasing the amounts of certain natural substances in the brain that are needed to maintain mental balance.

Related Packages: 70934-0071-30
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Amitriptyline

Product Information

NDC	70934-0071
Product ID	70934-071_f14f1d36-f9c8-1669-e053-2995a90a05a3
Associated GPIs	58200010100310
GCN Sequence Number	046046
GCN Sequence Number Description	amitriptyline HCl TABLET 25 MG ORAL
HIC3	H2U
HIC3 Description	TRICYCLIC ANTIDEPRESSANTS,REL.NON-SEL.REUPT-INHIB
GCN	16515
HICL Sequence Number	001643
HICL Sequence Number Description	AMITRIPTYLINE HCL
Brand/Generic	Generic
Proprietary Name	AMITRIPTYLINE HYDROCHLORIDE
Proprietary Name Suffix	n/a
Non-Proprietary Name	AMITRIPTYLINE HYDROCHLORIDE
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	25
Active Ingredient Units	mg/1
Substance Name	AMITRIPTYLINE HYDROCHLORIDE
Labeler Name	Denton Pharma, Inc. DBA Northwind Pharmaceuticals
Pharmaceutical Class	Tricyclic Antidepressant [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA202446
Listing Certified Through	n/a

Package

NDC 70934-0071-30 (70934007130)

Pricing Information	N/A
NDC Package Code	70934-071-30
Billing NDC	70934007130
Package	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-071-30)
Marketing Start Date	2018-01-25
NDC Exclude Flag	N