Package 68071-3878-9

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3878-9
Digits Only 6807138789
Product NDC 68071-3878
Product ID 68071-3878_3aff7330-cc8b-fa0f-e063-6294a90aa751
Description

90 TABLET, FILM COATED in 1 BOTTLE (68071-3878-9)

Marketing

Marketing Status
Marketed Since 2025-07-28
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": "3aff7330-cc8b-fa0f-e063-6294a90aa751", "openfda": {"upc": ["0368071387896"], "unii": ["1GEV3BAW9J"], "rxcui": ["896762"], "spl_set_id": ["3aff731f-1eec-19b5-e063-6294a90a3143"], "manufacturer_name": ["NuCare Pharmaceuticals , Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-3878-9)", "package_ndc": "68071-3878-9", "marketing_start_date": "20250728"}], "brand_name": "Labetalol Hydrochloride", "product_id": "68071-3878_3aff7330-cc8b-fa0f-e063-6294a90aa751", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68071-3878", "generic_name": "Labetalol Hydrochloride", "labeler_name": "NuCare Pharmaceuticals , Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA209603", "marketing_category": "ANDA", "marketing_start_date": "20210527", "listing_expiration_date": "20261231"}