propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: avkare
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler avkare
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

propranolol hydrochloride 80 mg/1

Manufacturer
AvKARE

Identifiers & Regulatory

Product NDC 42291-523
Product ID 42291-523_4b93e61b-2f17-4421-e063-6394a90ae3f3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078703
Listing Expiration 2027-12-31
Marketing Start 2017-05-16

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42291523
Hyphenated Format 42291-523

Supplemental Identifiers

RxCUI
856460 856481 856535 856569
UNII
F8A3652H1V

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
  • 80 mg/1
source: ndc
Packaging
  • 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42291-523-01)
  • 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42291-523-10)
source: ndc

Packages (2)

42291-523-01 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42291-523-01) 42291-523-10 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42291-523-10)

Ingredients (1)

propranolol hydrochloride (80 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": "4b93e61b-2f17-4421-e063-6394a90ae3f3", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856460", "856481", "856535", "856569"], "spl_set_id": ["753ab3cb-e7ee-424b-aa7d-195b5871a40e"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42291-523-01)", "package_ndc": "42291-523-01", "marketing_start_date": "20170516"}, {"sample": false, "description": "1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42291-523-10)", "package_ndc": "42291-523-10", "marketing_start_date": "20170731"}], "brand_name": "propranolol hydrochloride", "product_id": "42291-523_4b93e61b-2f17-4421-e063-6394a90ae3f3", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "42291-523", "generic_name": "propranolol hydrochloride", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "propranolol hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA078703", "marketing_category": "ANDA", "marketing_start_date": "20170516", "listing_expiration_date": "20271231"}