United States · FDA National Drug Code directory

Propranolol 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: 68788-8595_b5856c16-02a4-4034-8c3b-5250dc4eddea
Product NDC: 68788-8595
Form: TABLET
Composition / generic term: Propranolol Hydrochloride
Labeler: Preferred Pharmaceuticals Inc.
Marketing category: ANDA
Marketing start / end (source format): 20240301
Source listing expiry: 20271231

Source-listed ingredients

PROPRANOLOL HYDROCHLORIDE — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET in 1 BOTTLE (68788-8595-3) · 68788-8595-3
90 TABLET in 1 BOTTLE (68788-8595-9) · 68788-8595-9

Source and coverage

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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.

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