United States · FDA National Drug Code directory

Imipramine Hydrochloride

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 64380-170_567e586c-d32c-4362-b75f-a2c3a5a19352
Product NDC: 64380-170
Form: TABLET
Composition / generic term: Imipramine Hydrochloride
Labeler: Strides Pharma Science Limited
Marketing category: ANDA
Marketing start / end (source format): 20220509
Source listing expiry: 20271231

Source-listed ingredients

IMIPRAMINE HYDROCHLORIDE — 25 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

100 TABLET in 1 BOTTLE, PLASTIC (64380-170-01) · 64380-170-01
1000 TABLET in 1 BOTTLE, PLASTIC (64380-170-02) · 64380-170-02

Source and coverage

Open FDA National Drug Code directory →

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →