vancomycin hydrochloride
Generic: vancomycin hydrochloride
Labeler: meitheal pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
vancomycin hydrochloride
Generic Name
vancomycin hydrochloride
Labeler
meitheal pharmaceuticals inc.
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
vancomycin hydrochloride 750 mg/15mL
Manufacturer
Identifiers & Regulatory
Product NDC
71288-024
Product ID
71288-024_c050d3db-83fa-4e01-a304-db41eb41086a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA215195
Listing Expiration
2026-12-31
Marketing Start
2022-09-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71288024
Hyphenated Format
71288-024
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
ANDA215195 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 750 mg/15mL
Packaging
- 10 VIAL, SINGLE-DOSE in 1 CARTON (71288-024-21) / 15 mL in 1 VIAL, SINGLE-DOSE (71288-024-20)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "c050d3db-83fa-4e01-a304-db41eb41086a", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["1807518"], "spl_set_id": ["e5e26614-4119-40cc-b092-48ab97a41287"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (71288-024-21) / 15 mL in 1 VIAL, SINGLE-DOSE (71288-024-20)", "package_ndc": "71288-024-21", "marketing_start_date": "20220915"}], "brand_name": "Vancomycin hydrochloride", "product_id": "71288-024_c050d3db-83fa-4e01-a304-db41eb41086a", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "71288-024", "generic_name": "Vancomycin hydrochloride", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vancomycin hydrochloride", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "750 mg/15mL"}], "application_number": "ANDA215195", "marketing_category": "ANDA", "marketing_start_date": "20220915", "listing_expiration_date": "20261231"}