propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

propranolol hydrochloride 40 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-647
Product ID 43063-647_2f3b1710-4cbb-8df1-e063-6294a90a7539
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 43063647
Hyphenated Format 43063-647

Supplemental Identifiers

RxCUI
856519
UPC
0343063647905
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 ANDA070221 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (43063-647-30)
  • 90 TABLET in 1 BOTTLE, PLASTIC (43063-647-90)
source: ndc

Packages (2)

43063-647-30 30 TABLET in 1 BOTTLE, PLASTIC (43063-647-30) 43063-647-90 90 TABLET in 1 BOTTLE, PLASTIC (43063-647-90)

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": "2f3b1710-4cbb-8df1-e063-6294a90a7539", "openfda": {"upc": ["0343063647905"], "unii": ["F8A3652H1V"], "rxcui": ["856519"], "spl_set_id": ["29a3a271-dabc-437f-e054-00144ff8d46c"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-647-30)", "package_ndc": "43063-647-30", "marketing_start_date": "20160309"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-647-90)", "package_ndc": "43063-647-90", "marketing_start_date": "20160309"}], "brand_name": "Propranolol Hydrochloride", "product_id": "43063-647_2f3b1710-4cbb-8df1-e063-6294a90a7539", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "43063-647", "generic_name": "propranolol hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, 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"}