vancomycin

Generic: vancomycin hydrochloride

Labeler: sagent pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name vancomycin
Generic Name vancomycin hydrochloride
Labeler sagent pharmaceuticals
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

vancomycin hydrochloride 10 g/100mL

Manufacturer
Sagent Pharmaceuticals

Identifiers & Regulatory

Product NDC 25021-158
Product ID 25021-158_9b6f6171-cd0c-4468-a018-ebec650749ab
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200837
Listing Expiration 2026-12-31
Marketing Start 2012-09-20

Pharmacologic Class

Classes
glycopeptide antibacterial [epc] glycopeptides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 25021158
Hyphenated Format 25021-158

Supplemental Identifiers

RxCUI
239209 313572
UNII
71WO621TJD

Packaging Origin

Original Packager
true

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 (source: ndc)
Generic Name vancomycin hydrochloride (source: ndc)
Application Number ANDA200837 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 g/100mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (25021-158-99) / 100 mL in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (1)

vancomycin hydrochloride (10 g/100mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "9b6f6171-cd0c-4468-a018-ebec650749ab", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["239209", "313572"], "spl_set_id": ["06dcfd36-942f-4752-86ad-4c5a6fc3e48f"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (25021-158-99)  / 100 mL in 1 BOTTLE", "package_ndc": "25021-158-99", "marketing_start_date": "20120920"}], "brand_name": "Vancomycin", "product_id": "25021-158_9b6f6171-cd0c-4468-a018-ebec650749ab", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "25021-158", "generic_name": "vancomycin hydrochloride", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vancomycin", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "10 g/100mL"}], "application_number": "ANDA200837", "marketing_category": "ANDA", "marketing_start_date": "20120920", "listing_expiration_date": "20261231"}