Package 50090-1290-0
Brand: labetalol hcl
Generic: labetalol hydrochloridePackage Facts
Identity
Package NDC
50090-1290-0
Digits Only
5009012900
Product NDC
50090-1290
Description
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-1290-0)
Marketing
Marketing Status
Brand
labetalol hcl
Generic
labetalol hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0797ccb6-b00c-4ee4-91f3-a55705048b96", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896758", "896762", "896766"], "spl_set_id": ["312dde0d-5147-483e-968f-4e0d46114176"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-1290-0)", "package_ndc": "50090-1290-0", "marketing_start_date": "20141128"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-1290-1)", "package_ndc": "50090-1290-1", "marketing_start_date": "20150806"}], "brand_name": "Labetalol HCL", "product_id": "50090-1290_0797ccb6-b00c-4ee4-91f3-a55705048b96", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-1290", "generic_name": "Labetalol Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol HCL", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA200908", "marketing_category": "ANDA", "marketing_start_date": "20120724", "listing_expiration_date": "20261231"}