propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: aphena pharma solutions - tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler aphena pharma solutions - tennessee, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

propranolol hydrochloride 20 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-339
Product ID 71610-339_c8c0bd51-a7c2-4d89-bee2-063cd4da43f3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070213
Listing Expiration 2026-12-31
Marketing Start 1985-11-19

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71610339
Hyphenated Format 71610-339

Supplemental Identifiers

RxCUI
856457
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 ANDA070213 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 45 TABLET in 1 BOTTLE, PLASTIC (71610-339-45)
  • 90 TABLET in 1 BOTTLE, PLASTIC (71610-339-60)
source: ndc

Packages (2)

71610-339-45 45 TABLET in 1 BOTTLE, PLASTIC (71610-339-45) 71610-339-60 90 TABLET in 1 BOTTLE, PLASTIC (71610-339-60)

Ingredients (1)

propranolol hydrochloride (20 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": "c8c0bd51-a7c2-4d89-bee2-063cd4da43f3", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856457"], "spl_set_id": ["3c05ab1f-05b0-494a-b640-667e7cf517a1"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "45 TABLET in 1 BOTTLE, PLASTIC (71610-339-45)", "package_ndc": "71610-339-45", "marketing_start_date": "20210507"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (71610-339-60)", "package_ndc": "71610-339-60", "marketing_start_date": "20190820"}], "brand_name": "Propranolol Hydrochloride", "product_id": "71610-339_c8c0bd51-a7c2-4d89-bee2-063cd4da43f3", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71610-339", "generic_name": "propranolol hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA070213", "marketing_category": "ANDA", "marketing_start_date": "19851119", "listing_expiration_date": "20261231"}