Package 72266-103-01

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72266-103-01
Digits Only 7226610301
Product NDC 72266-103
Product ID 72266-103_189abc58-65af-e772-e063-6394a90a5ed3
Description

1 VIAL, MULTI-DOSE in 1 CARTON (72266-103-01) / 40 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2019-04-02
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": "189abc58-65af-e772-e063-6394a90a5ed3", "openfda": {"upc": ["0372266103017", "0372266102010"], "unii": ["1GEV3BAW9J"], "rxcui": ["896771"], "spl_set_id": ["4a5ffab2-a3b8-411e-992d-7f38d508643a"], "manufacturer_name": ["Fosun Pharma USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (72266-103-01)  / 40 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "72266-103-01", "marketing_start_date": "20190402"}], "brand_name": "Labetalol Hydrochloride", "product_id": "72266-103_189abc58-65af-e772-e063-6394a90a5ed3", "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": "20190402", "listing_expiration_date": "20261231"}