Package 68180-167-13

Brand: vancomycin hydrochloride

Generic: vancomycin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68180-167-13
Digits Only 6818016713
Product NDC 68180-167
Description

2 BLISTER PACK in 1 CARTON (68180-167-13) / 10 CAPSULE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2015-03-27
Brand vancomycin hydrochloride
Generic vancomycin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cf4678a5-2147-44e8-80c2-2a5c699140b6", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["313570", "313571"], "spl_set_id": ["20a8f14c-9c90-47f7-98b1-e8c63414cdf0"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (68180-167-13)  / 10 CAPSULE in 1 BLISTER PACK", "package_ndc": "68180-167-13", "marketing_start_date": "20150327"}], "brand_name": "VANCOMYCIN HYDROCHLORIDE", "product_id": "68180-167_cf4678a5-2147-44e8-80c2-2a5c699140b6", "dosage_form": "CAPSULE", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "68180-167", "generic_name": "VANCOMYCIN HYDROCHLORIDE", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VANCOMYCIN HYDROCHLORIDE", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA090439", "marketing_category": "ANDA", "marketing_start_date": "20150327", "listing_expiration_date": "20261231"}