propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: amici pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler amici pharmaceuticals llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

propranolol hydrochloride 40 mg/1

Manufacturer
AMICI PHARMACEUTICALS LLC

Identifiers & Regulatory

Product NDC 69292-534
Product ID 69292-534_ce606d4c-3af5-4274-b843-d8d8fe2c96ab
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070322
Listing Expiration 2026-12-31
Marketing Start 2019-10-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69292534
Hyphenated Format 69292-534

Supplemental Identifiers

RxCUI
856448 856457 856519 856556 856578
UPC
0369292534014 0369292538012 0369292532010 0369292530016 0369292536018
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 ANDA070322 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (69292-534-01)
  • 1000 TABLET in 1 BOTTLE (69292-534-10)
source: ndc

Packages (2)

69292-534-01 100 TABLET in 1 BOTTLE (69292-534-01) 69292-534-10 1000 TABLET in 1 BOTTLE (69292-534-10)

Ingredients (1)

propranolol hydrochloride (40 mg/1)

Linked Drug Pages (1)

Propranolol Hydrochloride, Propranolol hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ce606d4c-3af5-4274-b843-d8d8fe2c96ab", "openfda": {"upc": ["0369292534014", "0369292538012", "0369292532010", "0369292530016", "0369292536018"], "unii": ["F8A3652H1V"], "rxcui": ["856448", "856457", "856519", "856556", "856578"], "spl_set_id": ["8efc9fc6-6db0-43c9-892b-7423a9ba679f"], "manufacturer_name": ["AMICI PHARMACEUTICALS LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69292-534-01)", "package_ndc": "69292-534-01", "marketing_start_date": "20191031"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (69292-534-10)", "package_ndc": "69292-534-10", "marketing_start_date": "20191031"}], "brand_name": "Propranolol Hydrochloride", "product_id": "69292-534_ce606d4c-3af5-4274-b843-d8d8fe2c96ab", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "69292-534", "generic_name": "Propranolol Hydrochloride", "labeler_name": "AMICI PHARMACEUTICALS LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA070322", "marketing_category": "ANDA", "marketing_start_date": "20191031", "listing_expiration_date": "20261231"}