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 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72162-2306
Product ID
72162-2306_91d9dc98-b742-4507-aea8-988c8bf4e6b3
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
721622306
Hyphenated Format
72162-2306
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
- 250 mg/1
Packaging
- 50 CAPSULE in 1 BOTTLE (72162-2306-4)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "91d9dc98-b742-4507-aea8-988c8bf4e6b3", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["313571"], "spl_set_id": ["7bbd2c81-33d9-4397-8795-8b9fa28cb5cf"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "50 CAPSULE in 1 BOTTLE (72162-2306-4)", "package_ndc": "72162-2306-4", "marketing_start_date": "20240513"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "72162-2306_91d9dc98-b742-4507-aea8-988c8bf4e6b3", "dosage_form": "CAPSULE", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "72162-2306", "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": "250 mg/1"}], "application_number": "ANDA210729", "marketing_category": "ANDA", "marketing_start_date": "20240115", "listing_expiration_date": "20261231"}