vancomycin hydrochloride

Generic: vancomycin hydrochloride

Labeler: civica, inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

vancomycin hydrochloride 1 g/1

Manufacturer
Civica, Inc

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
glycopeptide antibacterial [epc] glycopeptides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72572029
Hyphenated Format 72572-029

Supplemental Identifiers

RxCUI
1807513
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 hydrochloride (source: ndc)
Generic Name vancomycin hydrochloride (source: ndc)
Application Number ANDA062912 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
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)
source: ndc

Packages (1)

Ingredients (1)

vancomycin hydrochloride (1 g/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"}