sterile water

Generic: sterile water

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name sterile water
Generic Name sterile water
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION
Routes
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active Ingredients

water 1 mL/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1329
Product ID 51662-1329_2b4b1249-227f-4d64-e063-6294a90a8f8d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018801
Listing Expiration 2026-12-31
Marketing Start 2018-10-08

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621329
Hyphenated Format 51662-1329

Supplemental Identifiers

UNII
059QF0KO0R

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 NDA018801 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 1 mL/mL
source: ndc
Packaging
  • 10 mL in 1 VIAL, PLASTIC (51662-1329-1)
source: ndc

Packages (1)

Ingredients (1)

water (1 mL/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "2b4b1249-227f-4d64-e063-6294a90a8f8d", "openfda": {"unii": ["059QF0KO0R"], "spl_set_id": ["77bd3c0f-f4ab-7cfa-e053-2a91aa0a1b83"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 VIAL, PLASTIC (51662-1329-1)", "package_ndc": "51662-1329-1", "marketing_start_date": "20181008"}], "brand_name": "STERILE WATER", "product_id": "51662-1329_2b4b1249-227f-4d64-e063-6294a90a8f8d", "dosage_form": "INJECTION", "product_ndc": "51662-1329", "generic_name": "STERILE WATER", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "STERILE WATER", "active_ingredients": [{"name": "WATER", "strength": "1 mL/mL"}], "application_number": "NDA018801", "marketing_category": "NDA", "marketing_start_date": "20181008", "listing_expiration_date": "20261231"}