NDC 82619-135 – Propranolol Hydrochloride

Propranolol Hydrochloride 160 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug

Product NDC82619-135

Product details

Brand name
Propranolol Hydrochloride
Generic name
Propranolol Hydrochloride
Labeler
Creekwood Pharmaceuticals LLC
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA219460
Marketed since
August 29, 2026
Listing expires
December 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Propranolol Hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
82619-135-01100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82619-135-01)Aug 29, 2026
82619-135-02500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82619-135-02)Aug 29, 2026

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