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 43353-961
Product ID 43353-961_49006163-8921-6eaf-e063-6394a90a39c2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070213
Listing Expiration 2027-12-31
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 43353961
Hyphenated Format 43353-961

Supplemental Identifiers

RxCUI
856457 856519
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
  • 90 TABLET in 1 BOTTLE, PLASTIC (43353-961-60)
source: ndc

Packages (1)

Ingredients (1)

propranolol hydrochloride (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "49006163-8921-6eaf-e063-6394a90a39c2", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856457", "856519"], "spl_set_id": ["7da9bb37-cc22-4eff-8de0-429f64cb599e"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43353-961-60)", "package_ndc": "43353-961-60", "marketing_start_date": "20140911"}], "brand_name": "Propranolol Hydrochloride", "product_id": "43353-961_49006163-8921-6eaf-e063-6394a90a39c2", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "43353-961", "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": "20271231"}