Package 0591-0605-05

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0591-0605-05
Digits Only 0591060505
Product NDC 0591-0605
Product ID 0591-0605_d5dfcb69-d2c4-49ca-a684-83c9e15b3b06
Description

500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0605-05)

Marketing

Marketing Status
Discontinued 2026-09-30
Brand labetalol hydrochloride
Generic labetalol hydrochloride
Sample Package No

Linked Drug Pages (1)

Labetalol hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d5dfcb69-d2c4-49ca-a684-83c9e15b3b06", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896758", "896762", "896766"], "spl_set_id": ["a5b65a9b-6b8a-48a4-9c72-0e605bb309eb"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0605-01)", "package_ndc": "0591-0605-01", "marketing_end_date": "20260930", "marketing_start_date": "19980803"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0605-05)", "package_ndc": "0591-0605-05", "marketing_end_date": "20260930", "marketing_start_date": "19980803"}], "brand_name": "Labetalol hydrochloride", "product_id": "0591-0605_d5dfcb69-d2c4-49ca-a684-83c9e15b3b06", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0591-0605", "generic_name": "Labetalol hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA075133", "marketing_category": "ANDA", "marketing_end_date": "20260930", "marketing_start_date": "19980803"}