propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

propranolol hydrochloride 20 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7468
Product ID 0904-7468_b9cee427-7372-4b05-9d11-b6d1371f8081
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071972
Listing Expiration 2026-12-31
Marketing Start 2024-09-20

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09047468
Hyphenated Format 0904-7468

Supplemental Identifiers

RxCUI
856448 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 ANDA071972 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 50 BLISTER PACK in 1 CARTON (0904-7468-06) / 1 TABLET in 1 BLISTER PACK
  • 100 BLISTER PACK in 1 CARTON (0904-7468-61) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (2)

0904-7468-06 50 BLISTER PACK in 1 CARTON (0904-7468-06) / 1 TABLET in 1 BLISTER PACK 0904-7468-61 100 BLISTER PACK in 1 CARTON (0904-7468-61) / 1 TABLET in 1 BLISTER PACK

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": "b9cee427-7372-4b05-9d11-b6d1371f8081", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856448", "856457"], "spl_set_id": ["e7218c9b-b9b8-4cf0-a2c7-c759ad3a65ba"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 CARTON (0904-7468-06)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7468-06", "marketing_start_date": "20240920"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7468-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7468-61", "marketing_start_date": "20240920"}], "brand_name": "Propranolol Hydrochloride", "product_id": "0904-7468_b9cee427-7372-4b05-9d11-b6d1371f8081", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0904-7468", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA071972", "marketing_category": "ANDA", "marketing_start_date": "20240920", "listing_expiration_date": "20261231"}