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NDC 43063-0822-30 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 PD-Rx Pharmaceuticals, Inc.. 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: 43063-0822-30
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Amitriptyline

Product Information

NDC	43063-0822
Product ID	43063-822_fa69db8c-7af0-8f5b-e053-6294a90af7e1
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	PD-Rx Pharmaceuticals, Inc.
Pharmaceutical Class	Tricyclic Antidepressant [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA085966
Listing Certified Through	2024-12-31

Package

NDC 43063-0822-30 (43063082230)

Pricing Information	N/A
NDC Package Code	43063-822-30
Billing NDC	43063082230
Package	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-822-30)
Marketing Start Date	2018-01-08
NDC Exclude Flag	N