Package 62135-800-60

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62135-800-60
Digits Only 6213580060
Product NDC 62135-800
Product ID 62135-800_44fde4f9-0088-6476-e063-6394a90a6a92
Description

60 TABLET in 1 BOTTLE (62135-800-60)

Marketing

Marketing Status
Marketed Since 2023-10-24
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": "44fde4f9-0088-6476-e063-6394a90a6a92", "openfda": {"upc": ["0362135791605", "0362135800604", "0362135792602"], "unii": ["1GEV3BAW9J"], "rxcui": ["896758", "896762", "896766"], "spl_set_id": ["ac439c08-1e47-4306-8308-b31d7a1a443c"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (62135-800-60)", "package_ndc": "62135-800-60", "marketing_start_date": "20231024"}], "brand_name": "Labetalol Hydrochloride", "product_id": "62135-800_44fde4f9-0088-6476-e063-6394a90a6a92", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "62135-800", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA074787", "marketing_category": "ANDA", "marketing_start_date": "20200222", "listing_expiration_date": "20261231"}