vancomycin hydrochloride
Generic: vancomycin hydrochloride
Labeler: civica, incDrug Facts
Product Profile
Brand Name
vancomycin hydrochloride
Generic Name
vancomycin hydrochloride
Labeler
civica, inc
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
vancomycin hydrochloride 1 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
72572-029
Product ID
72572-029_3e041ec6-811b-4f26-9303-959cb09d5f57
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA062912
Listing Expiration
2026-12-31
Marketing Start
2025-11-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72572029
Hyphenated Format
72572-029
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
ANDA062912 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/1
Packaging
- 10 VIAL, SINGLE-DOSE in 1 CARTON (72572-029-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (72572-029-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "3e041ec6-811b-4f26-9303-959cb09d5f57", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["1807513"], "spl_set_id": ["3e041ec6-811b-4f26-9303-959cb09d5f57"], "manufacturer_name": ["Civica, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (72572-029-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (72572-029-01)", "package_ndc": "72572-029-10", "marketing_start_date": "20251110"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "72572-029_3e041ec6-811b-4f26-9303-959cb09d5f57", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "72572-029", "generic_name": "VANCOMYCIN HYDROCHLORIDE", "labeler_name": "Civica, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vancomycin Hydrochloride", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "1 g/1"}], "application_number": "ANDA062912", "marketing_category": "ANDA", "marketing_start_date": "20251110", "listing_expiration_date": "20261231"}