vancomycin hydrochloride

Generic: vancomycin hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name vancomycin hydrochloride
Generic Name vancomycin hydrochloride
Labeler bryant ranch prepack
Dosage Form POWDER, FOR SOLUTION
Routes
ORAL
Active Ingredients

vancomycin hydrochloride 250 mg/5mL

Manufacturer
Bryant Ranch Prepack

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
glycopeptide antibacterial [epc] glycopeptides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352948
Hyphenated Format 71335-2948

Supplemental Identifiers

RxCUI
2000134
UNII
71WO621TJD

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/5mL
source: ndc
Packaging
  • 80 mL in 1 BOTTLE (71335-2948-1)
source: ndc

Packages (1)

Ingredients (1)

vancomycin hydrochloride (250 mg/5mL)

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"}