vancomycin hydrochloride
Generic: vancomycin hydrochloride
Labeler: sagent pharmaceuticalsDrug Facts
Product Profile
Brand Name
vancomycin hydrochloride
Generic Name
vancomycin hydrochloride
Labeler
sagent pharmaceuticals
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
vancomycin hydrochloride 1.5 g/30mL
Manufacturer
Identifiers & Regulatory
Product NDC
25021-149
Product ID
25021-149_a05d9267-0d03-44f5-ae26-e7a523b5b862
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA218140
Listing Expiration
2026-12-31
Marketing Start
2025-06-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
25021149
Hyphenated Format
25021-149
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 hydrochloride (source: ndc)
Generic Name
vancomycin hydrochloride (source: ndc)
Application Number
ANDA218140 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1.5 g/30mL
Packaging
- 10 VIAL in 1 CARTON (25021-149-30) / 30 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "a05d9267-0d03-44f5-ae26-e7a523b5b862", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["1807518", "2049888", "2049890"], "spl_set_id": ["f623889c-a47a-4b3a-b3a9-e04051f5c2df"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-149-30) / 30 mL in 1 VIAL", "package_ndc": "25021-149-30", "marketing_start_date": "20250601"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "25021-149_a05d9267-0d03-44f5-ae26-e7a523b5b862", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "25021-149", "generic_name": "Vancomycin Hydrochloride", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vancomycin Hydrochloride", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "1.5 g/30mL"}], "application_number": "ANDA218140", "marketing_category": "ANDA", "marketing_start_date": "20250601", "listing_expiration_date": "20261231"}