vancomycin hydrochloride
Generic: vancomycin hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
vancomycin hydrochloride
Generic Name
vancomycin hydrochloride
Labeler
bryant ranch prepack
Dosage Form
POWDER, FOR SOLUTION
Routes
Active Ingredients
vancomycin hydrochloride 250 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
71335-2948
Product ID
71335-2948_bbbbe78c-d261-4630-8abb-b653a6f9a479
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA061667
Listing Expiration
2026-12-31
Marketing Start
2019-09-09
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713352948
Hyphenated Format
71335-2948
Supplemental Identifiers
RxCUI
UNII
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
ANDA061667 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/5mL
Packaging
- 80 mL in 1 BOTTLE (71335-2948-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bbbbe78c-d261-4630-8abb-b653a6f9a479", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["2000134"], "spl_set_id": ["8193f588-a032-451e-a0a1-819a5ea834c8"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "80 mL in 1 BOTTLE (71335-2948-1)", "package_ndc": "71335-2948-1", "marketing_start_date": "20251106"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "71335-2948_bbbbe78c-d261-4630-8abb-b653a6f9a479", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "71335-2948", "generic_name": "Vancomycin Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vancomycin Hydrochloride", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "250 mg/5mL"}], "application_number": "ANDA061667", "marketing_category": "ANDA", "marketing_start_date": "20190909", "listing_expiration_date": "20261231"}