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NDC 70934-0607-90 AMITRIPTYLINE HYDROCHLORIDE 50 mg/1 Details

AMITRIPTYLINE HYDROCHLORIDE 50 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: 70934-0607-90
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Amitriptyline

Product Information

NDC	70934-0607
Product ID	70934-607_ab725a6d-3e1d-70ee-e053-2995a90a5044
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
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	50
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	2022-12-31

Package

NDC 70934-0607-90 (70934060790)

Pricing Information	N/A
NDC Package Code	70934-607-90
Billing NDC	70934060790
Package	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-607-90)
Marketing Start Date	2020-05-20
NDC Exclude Flag	N