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
- 17856-8728_40333fbc-1ccd-7a2c-e063-6294a90a8bc9
- Product NDC
- 17856-8728
- Form
- SOLUTION
- Composition / generic term
- Propranolol Hydrochloride
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19870515
- Source listing expiry
- 20261231
Source-listed ingredients
- PROPRANOLOL HYDROCHLORIDE — 20 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 50 CUP in 1 CASE (17856-8728-1) / 5 mL in 1 CUP · 17856-8728-1
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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