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 10 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 66267-261
Product ID 66267-261_1fa6afe6-d920-02d3-e063-6394a90a41c7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070217
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 66267261
Hyphenated Format 66267-261

Supplemental Identifiers

RxCUI
856448
UPC
0366267261906
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 ANDA070217 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (66267-261-90)
source: ndc

Packages (1)

66267-261-90 90 TABLET in 1 BOTTLE (66267-261-90)

Ingredients (1)

propranolol hydrochloride (10 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": "1fa6afe6-d920-02d3-e063-6394a90a41c7", "openfda": {"upc": ["0366267261906"], "unii": ["F8A3652H1V"], "rxcui": ["856448"], "spl_set_id": ["92c4bd8f-d0e6-d11a-e053-2995a90a635d"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (66267-261-90)", "package_ndc": "66267-261-90", "marketing_start_date": "20190917"}], "brand_name": "Propranolol Hydrochloride", "product_id": "66267-261_1fa6afe6-d920-02d3-e063-6394a90a41c7", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "66267-261", "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": "10 mg/1"}], "application_number": "ANDA070217", "marketing_category": "ANDA", "marketing_start_date": "20100621", "listing_expiration_date": "20261231"}