vancomycin hydrochloride
Generic: vancomycin hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
vancomycin hydrochloride
Generic Name
vancomycin hydrochloride
Labeler
bryant ranch prepack
Dosage Form
CAPSULE
Routes
Active Ingredients
vancomycin hydrochloride 125 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72162-2305
Product ID
72162-2305_38c75f1c-f29c-4671-aa99-f9d3f7c650ef
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210729
Listing Expiration
2026-12-31
Marketing Start
2024-01-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721622305
Hyphenated Format
72162-2305
Supplemental Identifiers
RxCUI
UNII
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
ANDA210729 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 125 mg/1
Packaging
- 50 CAPSULE in 1 BOTTLE (72162-2305-4)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "38c75f1c-f29c-4671-aa99-f9d3f7c650ef", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["313570"], "spl_set_id": ["d6b8147b-5f93-49ee-8b27-78fe58987c90"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "50 CAPSULE in 1 BOTTLE (72162-2305-4)", "package_ndc": "72162-2305-4", "marketing_start_date": "20240513"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "72162-2305_38c75f1c-f29c-4671-aa99-f9d3f7c650ef", "dosage_form": "CAPSULE", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "72162-2305", "generic_name": "Vancomycin Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vancomycin Hydrochloride", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "125 mg/1"}], "application_number": "ANDA210729", "marketing_category": "ANDA", "marketing_start_date": "20240115", "listing_expiration_date": "20261231"}