Package 68001-382-00

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68001-382-00
Digits Only 6800138200
Product NDC 68001-382
Product ID 68001-382_ffac2849-40b6-4e5b-e053-6394a90ae38b
Description

100 TABLET, FILM COATED in 1 BOTTLE (68001-382-00)

Marketing

Marketing Status
Marketed Since 2019-02-18
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": "ffac2849-40b6-4e5b-e053-6394a90ae38b", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896758", "896762", "896766"], "spl_set_id": ["63ede355-42ec-4c52-a941-51e5f6b35ed6"], "manufacturer_name": ["BluePoint Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68001-382-00)", "package_ndc": "68001-382-00", "marketing_start_date": "20190218"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (68001-382-03)", "package_ndc": "68001-382-03", "marketing_start_date": "20190218"}], "brand_name": "Labetalol Hydrochloride", "product_id": "68001-382_ffac2849-40b6-4e5b-e053-6394a90ae38b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68001-382", "generic_name": "Labetalol Hydrochloride", "labeler_name": "BluePoint Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA207743", "marketing_category": "ANDA", "marketing_start_date": "20190218", "listing_expiration_date": "20261231"}