propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: breckenridge pharmaceutical, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler breckenridge pharmaceutical, inc.
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

propranolol hydrochloride 160 mg/1

Manufacturer
Breckenridge Pharmaceutical, Inc.

Identifiers & Regulatory

Product NDC 51991-820
Product ID 51991-820_f7b4203a-c93c-47a2-9ad0-41df7d7a2c26
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078703
Listing Expiration 2026-12-31
Marketing Start 2013-03-11

Pharmacologic Class

Classes
adrenergic beta-antagonists [moa] beta-adrenergic blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51991820
Hyphenated Format 51991-820

Supplemental Identifiers

RxCUI
856460 856481 856535 856569
UPC
0351991819011 0351991818014 0351991820017
UNII
F8A3652H1V

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name propranolol hydrochloride (source: ndc)
Generic Name propranolol hydrochloride (source: ndc)
Application Number ANDA078703 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 160 mg/1
source: ndc
Packaging
  • 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51991-820-01)
  • 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51991-820-05)
source: ndc

Packages (2)

51991-820-01 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51991-820-01) 51991-820-05 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51991-820-05)

Ingredients (1)

propranolol hydrochloride (160 mg/1)

Linked Drug Pages (1)

propranolol hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f7b4203a-c93c-47a2-9ad0-41df7d7a2c26", "openfda": {"upc": ["0351991819011", "0351991818014", "0351991820017"], "unii": ["F8A3652H1V"], "rxcui": ["856460", "856481", "856535", "856569"], "spl_set_id": ["179e31a7-9956-4fba-9e9a-2ca28d37d42b"], "manufacturer_name": ["Breckenridge Pharmaceutical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51991-820-01)", "package_ndc": "51991-820-01", "marketing_start_date": "20130311"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51991-820-05)", "package_ndc": "51991-820-05", "marketing_start_date": "20130311"}], "brand_name": "propranolol hydrochloride", "product_id": "51991-820_f7b4203a-c93c-47a2-9ad0-41df7d7a2c26", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "51991-820", "generic_name": "propranolol hydrochloride", "labeler_name": "Breckenridge Pharmaceutical, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "propranolol hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "160 mg/1"}], "application_number": "ANDA078703", "marketing_category": "ANDA", "marketing_start_date": "20130311", "listing_expiration_date": "20261231"}