vancomycin
Generic: vancomycin hydrochloride
Labeler: sagent pharmaceuticalsDrug Facts
Product Profile
Brand Name
vancomycin
Generic Name
vancomycin hydrochloride
Labeler
sagent pharmaceuticals
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
vancomycin hydrochloride 10 g/100mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
25021158
Hyphenated Format
25021-158
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 (source: ndc)
Generic Name
vancomycin hydrochloride (source: ndc)
Application Number
ANDA200837 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 g/100mL
Packaging
- 1 BOTTLE in 1 CARTON (25021-158-99) / 100 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
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"}