Package 0009-0104-04
Brand: lincocin
Generic: lincomycin hydrochloridePackage Facts
Identity
Package NDC
0009-0104-04
Digits Only
0009010404
Product NDC
0009-0104
Description
1 VIAL in 1 CARTON (0009-0104-04) / 2 mL in 1 VIAL
Marketing
Marketing Status
Brand
lincocin
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": "7e2f3780-88ee-4971-a4ab-3d6cd972c42c", "openfda": {"upc": ["0300090107048", "0300090104047"], "unii": ["M6T05Z2B68"], "rxcui": ["102787", "239212"], "spl_set_id": ["c01906fa-2c73-4c13-9765-2fd06628d263"], "manufacturer_name": ["Pharmacia & Upjohn Company LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (0009-0104-04) / 2 mL in 1 VIAL", "package_ndc": "0009-0104-04", "marketing_start_date": "20230818"}], "brand_name": "Lincocin", "product_id": "0009-0104_7e2f3780-88ee-4971-a4ab-3d6cd972c42c", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "0009-0104", "generic_name": "lincomycin hydrochloride", "labeler_name": "Pharmacia & Upjohn Company LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lincocin", "active_ingredients": [{"name": "LINCOMYCIN HYDROCHLORIDE", "strength": "300 mg/mL"}], "application_number": "NDA050317", "marketing_category": "NDA", "marketing_start_date": "20230818", "listing_expiration_date": "20261231"}