Package 0904-7453-61

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-7453-61
Digits Only 0904745361
Product NDC 0904-7453
Product ID 0904-7453_25dba2c0-ab5f-48c1-8768-533d26a16b53
Description

100 BLISTER PACK in 1 CARTON (0904-7453-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2024-10-08
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": "25dba2c0-ab5f-48c1-8768-533d26a16b53", "openfda": {"unii": ["1GEV3BAW9J"], "spl_set_id": ["35b5fd32-581d-427b-9a13-b7a02846d21d"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7453-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-7453-61", "marketing_start_date": "20241008"}], "brand_name": "Labetalol Hydrochloride", "product_id": "0904-7453_25dba2c0-ab5f-48c1-8768-533d26a16b53", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0904-7453", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA209603", "marketing_category": "ANDA", "marketing_start_date": "20241008", "listing_expiration_date": "20271231"}