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
- 82619-134_598d91b8-2d91-47e7-e063-6294a90a248a
- Product NDC
- 82619-134
- Form
- CAPSULE, EXTENDED RELEASE
- Composition / generic term
- Propranolol Hydrochloride
- Labeler
- Creekwood Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260829
- Source listing expiry
- 20271231
Source-listed ingredients
- PROPRANOLOL HYDROCHLORIDE — 120 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82619-134-01) · 82619-134-01
- 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82619-134-02) · 82619-134-02
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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