Package 39822-0350-2

Brand: lincomycin

Generic: lincomycin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 39822-0350-2
Digits Only 3982203502
Product NDC 39822-0350
Description

10 VIAL in 1 CARTON (39822-0350-2) / 2 mL in 1 VIAL (39822-0350-1)

Marketing

Marketing Status
Marketed Since 2015-07-05
Brand lincomycin
Generic lincomycin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCONJUNCTIVAL"], "spl_id": "df369d62-f1a4-1a53-e053-2995a90abbf9", "openfda": {"unii": ["M6T05Z2B68"], "rxcui": ["239212"], "spl_set_id": ["61f4851d-d919-400d-912a-05eb9dca11d4"], "manufacturer_name": ["XGen Pharmaceuticals DJB, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (39822-0350-2)  / 2 mL in 1 VIAL (39822-0350-1)", "package_ndc": "39822-0350-2", "marketing_start_date": "20150705"}], "brand_name": "Lincomycin", "product_id": "39822-0350_df369d62-f1a4-1a53-e053-2995a90abbf9", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "39822-0350", "generic_name": "lincomycin hydrochloride", "labeler_name": "XGen Pharmaceuticals DJB, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lincomycin", "active_ingredients": [{"name": "LINCOMYCIN HYDROCHLORIDE", "strength": "300 mg/mL"}], "application_number": "ANDA201746", "marketing_category": "ANDA", "marketing_start_date": "20150705", "listing_expiration_date": "20261231"}