vancomycin hydrochloride
Generic: vancomycin hydrochloride
Labeler: camber pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
vancomycin hydrochloride
Generic Name
vancomycin hydrochloride
Labeler
camber pharmaceuticals, inc.
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
vancomycin hydrochloride 500 mg/10mL
Manufacturer
Identifiers & Regulatory
Product NDC
31722-210
Product ID
31722-210_e449bca2-14c8-ae21-e053-2a95a90a942b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216591
Listing Expiration
2026-12-31
Marketing Start
2022-07-06
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
31722210
Hyphenated Format
31722-210
Supplemental Identifiers
RxCUI
UPC
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
ANDA216591 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/10mL
Packaging
- 10 VIAL in 1 CARTON (31722-210-10) / 10 mL in 1 VIAL (31722-210-33)
- 25 VIAL in 1 CARTON (31722-210-32) / 10 mL in 1 VIAL (31722-210-33)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "e449bca2-14c8-ae21-e053-2a95a90a942b", "openfda": {"upc": ["0331722211338", "0331722210331", "0331722211109"], "unii": ["71WO621TJD"], "rxcui": ["1807513", "1807516"], "spl_set_id": ["3f5dacea-af40-4103-b128-c5e0c0c52fa1"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (31722-210-10) / 10 mL in 1 VIAL (31722-210-33)", "package_ndc": "31722-210-10", "marketing_start_date": "20220706"}, {"sample": false, "description": "25 VIAL in 1 CARTON (31722-210-32) / 10 mL in 1 VIAL (31722-210-33)", "package_ndc": "31722-210-32", "marketing_start_date": "20220706"}], "brand_name": "VANCOMYCIN HYDROCHLORIDE", "product_id": "31722-210_e449bca2-14c8-ae21-e053-2a95a90a942b", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "31722-210", "generic_name": "VANCOMYCIN HYDROCHLORIDE", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VANCOMYCIN HYDROCHLORIDE", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "500 mg/10mL"}], "application_number": "ANDA216591", "marketing_category": "ANDA", "marketing_start_date": "20220706", "listing_expiration_date": "20261231"}