Package 59651-566-01

Brand: dicloxacillin sodium

Generic: dicloxacillin sodium
NDC Package

Package Facts

Identity

Package NDC 59651-566-01
Digits Only 5965156601
Product NDC 59651-566
Product ID 59651-566_faee6e2d-1b9c-4121-bc22-41313539b366
Description

100 CAPSULE in 1 BOTTLE (59651-566-01)

Marketing

Marketing Status
Marketed Since 2022-09-23
Brand dicloxacillin sodium
Generic dicloxacillin sodium
Sample Package No

Linked Drug Pages (1)

DICLOXACILLIN SODIUM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "faee6e2d-1b9c-4121-bc22-41313539b366", "openfda": {"unii": ["4HZT2V9KX0"], "rxcui": ["197595", "197596"], "spl_set_id": ["9074b5a6-850c-4144-9097-bb21073ee54d"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (59651-566-01)", "package_ndc": "59651-566-01", "marketing_start_date": "20220923"}], "brand_name": "DICLOXACILLIN SODIUM", "product_id": "59651-566_faee6e2d-1b9c-4121-bc22-41313539b366", "dosage_form": "CAPSULE", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "59651-566", "generic_name": "DICLOXACILLIN SODIUM", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DICLOXACILLIN SODIUM", "active_ingredients": [{"name": "DICLOXACILLIN SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA216845", "marketing_category": "ANDA", "marketing_start_date": "20220923", "listing_expiration_date": "20261231"}