vancomycin hydrochloride
Generic: vancomycin hydrochloride
Labeler: lupin pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
vancomycin hydrochloride
Generic Name
vancomycin hydrochloride
Labeler
lupin pharmaceuticals, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
vancomycin hydrochloride 125 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68180-166
Product ID
68180-166_cf4678a5-2147-44e8-80c2-2a5c699140b6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090439
Listing Expiration
2026-12-31
Marketing Start
2015-03-27
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68180166
Hyphenated Format
68180-166
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
vancomycin hydrochloride (source: ndc)
Generic Name
vancomycin hydrochloride (source: ndc)
Application Number
ANDA090439 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 125 mg/1
Packaging
- 2 BLISTER PACK in 1 CARTON (68180-166-13) / 10 CAPSULE in 1 BLISTER PACK
Packages (1)
Ingredients (1)
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 (68180-166-13) / 10 CAPSULE in 1 BLISTER PACK", "package_ndc": "68180-166-13", "marketing_start_date": "20150327"}], "brand_name": "VANCOMYCIN HYDROCHLORIDE", "product_id": "68180-166_cf4678a5-2147-44e8-80c2-2a5c699140b6", "dosage_form": "CAPSULE", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "68180-166", "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": "125 mg/1"}], "application_number": "ANDA090439", "marketing_category": "ANDA", "marketing_start_date": "20150327", "listing_expiration_date": "20261231"}