propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: endo usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler endo usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

propranolol hydrochloride 40 mg/1

Manufacturer
Endo USA, Inc.

Identifiers & Regulatory

Product NDC 0603-5484
Product ID 0603-5484_2d7e19e5-6f01-4657-a201-829ea5a74f84
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070221
Listing Expiration 2026-12-31
Marketing Start 2010-06-21

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 06035484
Hyphenated Format 0603-5484

Supplemental Identifiers

RxCUI
856448 856457 856519 856556 856578
UPC
0306035482218 0306035485219 0306035483215 0306035486216 0306035484212
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 ANDA070221 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (0603-5484-21)
  • 1000 TABLET in 1 BOTTLE (0603-5484-32)
source: ndc

Packages (2)

0603-5484-21 100 TABLET in 1 BOTTLE (0603-5484-21) 0603-5484-32 1000 TABLET in 1 BOTTLE (0603-5484-32)

Ingredients (1)

propranolol hydrochloride (40 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": "2d7e19e5-6f01-4657-a201-829ea5a74f84", "openfda": {"upc": ["0306035482218", "0306035485219", "0306035483215", "0306035486216", "0306035484212"], "unii": ["F8A3652H1V"], "rxcui": ["856448", "856457", "856519", "856556", "856578"], "spl_set_id": ["0d74bb04-8227-4afa-b523-ce1556150e07"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0603-5484-21)", "package_ndc": "0603-5484-21", "marketing_start_date": "20100621"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (0603-5484-32)", "package_ndc": "0603-5484-32", "marketing_start_date": "20100621"}], "brand_name": "Propranolol Hydrochloride", "product_id": "0603-5484_2d7e19e5-6f01-4657-a201-829ea5a74f84", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0603-5484", "generic_name": "propranolol hydrochloride", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA070221", "marketing_category": "ANDA", "marketing_start_date": "20100621", "listing_expiration_date": "20261231"}