Package 36000-324-02

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 36000-324-02
Digits Only 3600032402
Product NDC 36000-324
Product ID 36000-324_219d4dec-02d1-4d4b-88fd-01b1dbad3abc
Description

1 VIAL in 1 CARTON (36000-324-02) / 40 mL in 1 VIAL (36000-324-01)

Marketing

Marketing Status
Marketed Since 2021-01-26
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": "219d4dec-02d1-4d4b-88fd-01b1dbad3abc", "openfda": {"upc": ["0336000324014", "0336000320016", "0336000322010"], "unii": ["1GEV3BAW9J"], "rxcui": ["896771", "2477889"], "spl_set_id": ["b17a7b3a-e7a5-4987-ae85-ad970e7540c7"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (36000-324-02)  / 40 mL in 1 VIAL (36000-324-01)", "package_ndc": "36000-324-02", "marketing_start_date": "20210126"}], "brand_name": "Labetalol Hydrochloride", "product_id": "36000-324_219d4dec-02d1-4d4b-88fd-01b1dbad3abc", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "36000-324", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA076051", "marketing_category": "ANDA", "marketing_start_date": "20210126", "listing_expiration_date": "20261231"}