propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: lannett company, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

propranolol hydrochloride 120 mg/1

Manufacturer
Lannett Company, Inc.

Identifiers & Regulatory

Product NDC 0527-4118
Product ID 0527-4118_ceeffec9-095b-4081-b268-7869b0685921
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212026
Listing Expiration 2026-12-31
Marketing Start 2020-01-06

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05274118
Hyphenated Format 0527-4118

Supplemental Identifiers

RxCUI
856460 856481 856535 856569
UPC
0305274116373
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 ANDA212026 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 120 mg/1
source: ndc
Packaging
  • 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-4118-37)
  • 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-4118-41)
source: ndc

Packages (2)

0527-4118-37 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-4118-37) 0527-4118-41 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-4118-41)

Ingredients (1)

propranolol hydrochloride (120 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": "ceeffec9-095b-4081-b268-7869b0685921", "openfda": {"upc": ["0305274116373"], "unii": ["F8A3652H1V"], "rxcui": ["856460", "856481", "856535", "856569"], "spl_set_id": ["5229b561-287b-463c-8679-cda4c34f440b"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-4118-37)", "package_ndc": "0527-4118-37", "marketing_start_date": "20200106"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-4118-41)", "package_ndc": "0527-4118-41", "marketing_start_date": "20200106"}], "brand_name": "Propranolol Hydrochloride", "product_id": "0527-4118_ceeffec9-095b-4081-b268-7869b0685921", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0527-4118", "generic_name": "propranolol hydrochloride", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA212026", "marketing_category": "ANDA", "marketing_start_date": "20200106", "listing_expiration_date": "20261231"}