sterile water
Generic: sterile water
Labeler: nephron pharmaceuticals corporationDrug Facts
Product Profile
Brand Name
sterile water
Generic Name
sterile water
Labeler
nephron pharmaceuticals corporation
Dosage Form
INJECTION
Routes
Active Ingredients
water 1 mL/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0487-6105
Product ID
0487-6105_39ada97d-53b0-5144-e063-6294a90a91ba
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211222
Listing Expiration
2026-12-31
Marketing Start
2021-06-07
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04876105
Hyphenated Format
0487-6105
Supplemental Identifiers
UPC
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
sterile water (source: ndc)
Generic Name
sterile water (source: ndc)
Application Number
ANDA211222 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mL/mL
Packaging
- 30 VIAL, PLASTIC in 1 CARTON (0487-6105-01) / 5 mL in 1 VIAL, PLASTIC
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "39ada97d-53b0-5144-e063-6294a90a91ba", "openfda": {"upc": ["0304876105013"], "unii": ["059QF0KO0R"], "spl_set_id": ["bc04a883-babc-87a6-e053-2995a90a3dfd"], "manufacturer_name": ["Nephron Pharmaceuticals Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 VIAL, PLASTIC in 1 CARTON (0487-6105-01) / 5 mL in 1 VIAL, PLASTIC", "package_ndc": "0487-6105-01", "marketing_start_date": "20210616"}], "brand_name": "Sterile Water", "product_id": "0487-6105_39ada97d-53b0-5144-e063-6294a90a91ba", "dosage_form": "INJECTION", "product_ndc": "0487-6105", "generic_name": "Sterile Water", "labeler_name": "Nephron Pharmaceuticals Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sterile Water", "active_ingredients": [{"name": "WATER", "strength": "1 mL/mL"}], "application_number": "ANDA211222", "marketing_category": "ANDA", "marketing_start_date": "20210607", "listing_expiration_date": "20261231"}