Propranolol Hydrochloride 51991-0817

Product NDC

51991-0817

Manufacturer: Breckenridge Pharmaceutical, Inc.
Dosage Form: Capsule, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: March 11, 2013
Listing Expires: December 31, 2026
Application: ANDA078703

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Active Ingredients

Ingredient	Strength
Propranolol Hydrochloride	60 mg/1

Drug Class

Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]

Packaging Options(2)

51991-0817-01

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51991-817-01)

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51991-0817-05

500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51991-817-05)

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