propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

propranolol hydrochloride 80 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-5071
Product ID 68071-5071_1b45506a-f5b5-08fa-e063-6394a90a5416
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 680715071
Hyphenated Format 68071-5071

Supplemental Identifiers

RxCUI
856578
UPC
0368071507119
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
  • 80 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68071-5071-1)
source: ndc

Packages (1)

68071-5071-1 100 TABLET in 1 BOTTLE (68071-5071-1)

Ingredients (1)

propranolol hydrochloride (80 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": "1b45506a-f5b5-08fa-e063-6394a90a5416", "openfda": {"upc": ["0368071507119"], "unii": ["F8A3652H1V"], "rxcui": ["856578"], "spl_set_id": ["933f792f-341f-4d71-e053-2a95a90ad341"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-5071-1)", "package_ndc": "68071-5071-1", "marketing_start_date": "20190923"}], "brand_name": "Propranolol Hydrochloride", "product_id": "68071-5071_1b45506a-f5b5-08fa-e063-6394a90a5416", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68071-5071", "generic_name": "propranolol hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA070221", "marketing_category": "ANDA", "marketing_start_date": "20100621", "listing_expiration_date": "20261231"}