Package 49884-122-05

Brand: labetalol hcl

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 49884-122-05
Digits Only 4988412205
Product NDC 49884-122
Product ID 49884-122_c44ec282-63ce-491d-8842-7050d099a6e4
Description

500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49884-122-05)

Marketing

Marketing Status
Discontinued 2026-03-31
Brand labetalol hcl
Generic labetalol hydrochloride
Sample Package No

Linked Drug Pages (1)

Labetalol HCL ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c44ec282-63ce-491d-8842-7050d099a6e4", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896758", "896762", "896766"], "spl_set_id": ["56ab2ff4-14a6-4297-afd8-56b92e1f64a0"], "manufacturer_name": ["Par Health USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49884-122-05)", "package_ndc": "49884-122-05", "marketing_end_date": "20260331", "marketing_start_date": "20120724"}], "brand_name": "Labetalol HCL", "product_id": "49884-122_c44ec282-63ce-491d-8842-7050d099a6e4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "49884-122", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Par Health USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol HCL", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA200908", "marketing_category": "ANDA", "marketing_end_date": "20260331", "marketing_start_date": "20120724"}