Package 60687-439-01

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-439-01
Digits Only 6068743901
Product NDC 60687-439
Product ID 60687-439_2a7ffcfa-7d3f-473c-e063-6394a90ad673
Description

100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-439-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-439-11)

Marketing

Marketing Status
Marketed Since 2019-07-16
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": "2a7ffcfa-7d3f-473c-e063-6394a90ad673", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896758", "896762", "896766"], "spl_set_id": ["3004aa59-288c-4971-b77b-78789715ef5a"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-439-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-439-11)", "package_ndc": "60687-439-01", "marketing_start_date": "20190716"}], "brand_name": "Labetalol Hydrochloride", "product_id": "60687-439_2a7ffcfa-7d3f-473c-e063-6394a90ad673", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "60687-439", "generic_name": "Labetalol Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA207743", "marketing_category": "ANDA", "marketing_start_date": "20190716", "listing_expiration_date": "20261231"}