labetalol hcl

Generic: labetalol hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name labetalol hcl
Generic Name labetalol hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

labetalol hydrochloride 300 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1410
Product ID 71335-1410_98b598e0-64b7-4a8c-9c7f-a8891fd4e708
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200908
Listing Expiration 2026-12-31
Marketing Start 2012-07-24

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713351410
Hyphenated Format 71335-1410

Supplemental Identifiers

RxCUI
896766
UNII
1GEV3BAW9J

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 labetalol hcl (source: ndc)
Generic Name labetalol hydrochloride (source: ndc)
Application Number ANDA200908 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-1410-1)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-1410-2)
  • 58 TABLET, FILM COATED in 1 BOTTLE (71335-1410-3)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-1410-4)
  • 180 TABLET, FILM COATED in 1 BOTTLE (71335-1410-5)
source: ndc

Packages (5)

71335-1410-1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1410-1) 71335-1410-2 60 TABLET, FILM COATED in 1 BOTTLE (71335-1410-2) 71335-1410-3 58 TABLET, FILM COATED in 1 BOTTLE (71335-1410-3) 71335-1410-4 90 TABLET, FILM COATED in 1 BOTTLE (71335-1410-4) 71335-1410-5 180 TABLET, FILM COATED in 1 BOTTLE (71335-1410-5)

Ingredients (1)

labetalol hydrochloride (300 mg/1)

Linked Drug Pages (1)

Labetalol HCL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "98b598e0-64b7-4a8c-9c7f-a8891fd4e708", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896766"], "spl_set_id": ["06ff81fe-9226-49a7-aa5c-f52b059d7cab"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1410-1)", "package_ndc": "71335-1410-1", "marketing_start_date": "20241007"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1410-2)", "package_ndc": "71335-1410-2", "marketing_start_date": "20191127"}, {"sample": false, "description": "58 TABLET, FILM COATED in 1 BOTTLE (71335-1410-3)", "package_ndc": "71335-1410-3", "marketing_start_date": "20241007"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-1410-4)", "package_ndc": "71335-1410-4", "marketing_start_date": "20241007"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71335-1410-5)", "package_ndc": "71335-1410-5", "marketing_start_date": "20241007"}], "brand_name": "Labetalol HCL", "product_id": "71335-1410_98b598e0-64b7-4a8c-9c7f-a8891fd4e708", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71335-1410", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol HCL", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA200908", "marketing_category": "ANDA", "marketing_start_date": "20120724", "listing_expiration_date": "20261231"}