Package 72266-103-41

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72266-103-41
Digits Only 7226610341
Product NDC 72266-103
Product ID 72266-103_2b363395-43e6-3aee-e063-6294a90a4e89
Description

1 VIAL, MULTI-DOSE in 1 CARTON (72266-103-41) / 40 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2021-03-31
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": ["INTRAVENOUS"], "spl_id": "2b363395-43e6-3aee-e063-6294a90a4e89", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896771"], "spl_set_id": ["f18dff28-f6f5-4ecb-9797-25062e247559"], "manufacturer_name": ["Fosun Pharma USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (72266-103-41)  / 40 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "72266-103-41", "marketing_start_date": "20210331"}], "brand_name": "Labetalol Hydrochloride", "product_id": "72266-103_2b363395-43e6-3aee-e063-6294a90a4e89", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72266-103", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Fosun Pharma USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA090699", "marketing_category": "ANDA", "marketing_start_date": "20210331", "listing_expiration_date": "20261231"}