Drugplain

Diltiazem Hydrochloride Extended-Release 120 mg/1

Diltiazem Hydrochloride · CAPSULE, EXTENDED RELEASE · Dr. Reddy's Labratories Inc.

10 Recalls on RecordCurrently in Shortage
Plain English

Diltiazem Hydrochloride Extended-Release is a capsule, extended release containing diltiazem hydrochloride at 120 mg/1, taken oral. Manufactured by Dr. Reddy's Labratories Inc..

Key Facts

Brand Name
Diltiazem Hydrochloride Extended-Release
Generic Name
Diltiazem Hydrochloride
NDC Code (Product)
75907-046
Manufacturer
Dr. Reddy's Labratories Inc.
Strength
120 mg/1
Dosage Form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Marketing Status
Application #
ANDA215775
Marketing Start
09/10/2024

Recall History

10 Recalls on Record
Class II11/01/2024

Glenmark Pharmaceuticals Inc., USA

cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above FDA recommended interim limit.

OngoingVoluntary: Firm initiated
Class III04/23/2018

Mckesson Packaging Services

Failed Dissolution Specifications. High dissolution results were obtained during stability testing.

TerminatedVoluntary: Firm initiated
Class II11/01/2024

Glenmark Pharmaceuticals Inc., USA

cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above FDA recommended interim limit.

OngoingVoluntary: Firm initiated
Class II11/01/2024

Glenmark Pharmaceuticals Inc., USA

cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above FDA recommended interim limit.

OngoingVoluntary: Firm initiated
Class III09/06/2019

Teva Pharmaceuticals USA

GMP Deviation: lot not intended for commercial distribution.

TerminatedVoluntary: Firm initiated
Class II03/26/2024

Glenmark Pharmaceuticals Inc., USA

Failed Dissolution Specifications: Out of Specification (OOS) was reported in test of dissolution at the 12th month time point in long term stability study.

OngoingVoluntary: Firm initiated
Class II01/13/2023

SUN PHARMACEUTICAL INDUSTRIES INC

Failed Impurity (Deacetyl Diltiazem Hydrochloride) specification during stability testing and failed dissolution testing at FDA laboratory.

TerminatedVoluntary: Firm initiated
Class II10/27/2021

Teva Pharmaceuticals USA

Labelling: Incorrect Exp. Date

TerminatedVoluntary: Firm initiated
Class II03/13/2025

Glenmark Pharmaceuticals Inc., USA

CGMP Deviations

OngoingVoluntary: Firm initiated
Class II07/21/2022

Teva Pharmaceuticals USA Inc

Failed Dissolution Specifications: below specification limits for dissolution.

TerminatedVoluntary: Firm initiated

Frequently Asked Questions

What is Diltiazem Hydrochloride Extended-Release used for?

Diltiazem Hydrochloride Extended-Release contains Diltiazem Hydrochloride. It is a capsule, extended release taken oral. Consult your doctor for specific uses.

Is Diltiazem Hydrochloride Extended-Release a controlled substance?

Diltiazem Hydrochloride Extended-Release is not classified as a controlled substance by the DEA.

What is the generic name for Diltiazem Hydrochloride Extended-Release?

The generic name for Diltiazem Hydrochloride Extended-Release is Diltiazem Hydrochloride. There are 12 other brand versions of Diltiazem Hydrochloride.

What is the NDC code for Diltiazem Hydrochloride Extended-Release 120 mg/1?

The NDC (National Drug Code) for Diltiazem Hydrochloride Extended-Release 120 mg/1 is 75907-046, listed by Dr. Reddy's Labratories Inc..