Package 55150-401-25

Brand: gentamicin

Generic: gentamicin
NDC Package

Package Facts

Identity

Package NDC 55150-401-25
Digits Only 5515040125
Product NDC 55150-401
Description

25 VIAL, SINGLE-DOSE in 1 CARTON (55150-401-25) / 2 mL in 1 VIAL, SINGLE-DOSE (55150-401-01)

Marketing

Marketing Status
Marketed Since 2024-01-08
Brand gentamicin
Generic gentamicin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "ec7eac4d-564f-4f16-b90a-a0c54d403056", "openfda": {"unii": ["8X7386QRLV"], "rxcui": ["1870676"], "spl_set_id": ["f8c608b3-50b8-4d5d-9e8a-e92c0d2e3cdc"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (55150-401-25)  / 2 mL in 1 VIAL, SINGLE-DOSE (55150-401-01)", "package_ndc": "55150-401-25", "marketing_start_date": "20240108"}], "brand_name": "Gentamicin", "product_id": "55150-401_ec7eac4d-564f-4f16-b90a-a0c54d403056", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Aminoglycoside Antibacterial [EPC]", "Aminoglycosides [CS]"], "product_ndc": "55150-401", "generic_name": "Gentamicin", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gentamicin", "active_ingredients": [{"name": "GENTAMICIN SULFATE", "strength": "10 mg/mL"}], "application_number": "ANDA215236", "marketing_category": "ANDA", "marketing_start_date": "20240108", "listing_expiration_date": "20271231"}