Package 70377-060-13
Brand: labetalol hydrochloride
Generic: labetalol hydrochloridePackage Facts
Identity
Package NDC
70377-060-13
Digits Only
7037706013
Product NDC
70377-060
Description
500 TABLET, FILM COATED in 1 BOTTLE (70377-060-13)
Marketing
Marketing Status
Brand
labetalol hydrochloride
Generic
labetalol hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f285cda1-e518-405e-9362-292ae2e14954", "openfda": {"upc": ["0370377061134", "0370377060120", "0370377063121", "0370377063114"], "unii": ["1GEV3BAW9J"], "rxcui": ["896758", "896762", "896766", "896983"], "spl_set_id": ["27e4ab03-c17b-4268-912c-e45a5e8f8dd8"], "manufacturer_name": ["Biocon Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (70377-060-11)", "package_ndc": "70377-060-11", "marketing_start_date": "20210527"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70377-060-12)", "package_ndc": "70377-060-12", "marketing_start_date": "20210527"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (70377-060-13)", "package_ndc": "70377-060-13", "marketing_start_date": "20210527"}], "brand_name": "Labetalol Hydrochloride", "product_id": "70377-060_f285cda1-e518-405e-9362-292ae2e14954", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70377-060", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Biocon Pharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA209603", "marketing_category": "ANDA", "marketing_start_date": "20210527", "listing_expiration_date": "20271231"}