Package 0121-1035-55

Brand: lincomycin

Generic: lincomycin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0121-1035-55
Digits Only 0121103555
Product NDC 0121-1035
Product ID 0121-1035_23f95ea6-ad32-a143-e063-6394a90ae77c
Description

10 VIAL, MULTI-DOSE in 1 CARTON (0121-1035-55) / 10 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2024-10-07
Brand lincomycin
Generic lincomycin hydrochloride
Sample Package No

Linked Drug Pages (1)

Lincomycin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "23f95ea6-ad32-a143-e063-6394a90ae77c", "openfda": {"unii": ["M6T05Z2B68"], "rxcui": ["239212"], "spl_set_id": ["23f9608c-3126-35db-e063-6294a90af054"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 CARTON (0121-1035-55)  / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "0121-1035-55", "marketing_start_date": "20241007"}], "brand_name": "Lincomycin", "product_id": "0121-1035_23f95ea6-ad32-a143-e063-6394a90ae77c", "dosage_form": "INJECTION", "product_ndc": "0121-1035", "generic_name": "Lincomycin Hydrochloride", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lincomycin", "active_ingredients": [{"name": "LINCOMYCIN HYDROCHLORIDE", "strength": "3000 mg/10mL"}], "application_number": "ANDA212770", "marketing_category": "ANDA", "marketing_start_date": "20241007", "listing_expiration_date": "20261231"}