sodium tetradecyl sulfate
Generic: sodium tetradecyl sulfate
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
sodium tetradecyl sulfate
Generic Name
sodium tetradecyl sulfate
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
tetradecyl hydrogen sulfate (ester) 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1562
Product ID
51662-1562_1203bbfe-c55f-1bcb-e063-6394a90a6577
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040541
Listing Expiration
2026-12-31
Marketing Start
2021-07-18
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621562
Hyphenated Format
51662-1562
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
sodium tetradecyl sulfate (source: ndc)
Generic Name
sodium tetradecyl sulfate (source: ndc)
Application Number
ANDA040541 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 2 mL in 1 VIAL, MULTI-DOSE (51662-1562-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "1203bbfe-c55f-1bcb-e063-6394a90a6577", "openfda": {"unii": ["6326W0DRHY"], "rxcui": ["204490"], "spl_set_id": ["c76f4b3b-9f93-349f-e053-2995a90a2d57"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "2 mL in 1 VIAL, MULTI-DOSE (51662-1562-1)", "package_ndc": "51662-1562-1", "marketing_start_date": "20210718"}], "brand_name": "SODIUM TETRADECYL SULFATE", "product_id": "51662-1562_1203bbfe-c55f-1bcb-e063-6394a90a6577", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "51662-1562", "generic_name": "SODIUM TETRADECYL SULFATE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM TETRADECYL SULFATE", "active_ingredients": [{"name": "TETRADECYL HYDROGEN SULFATE (ESTER)", "strength": "10 mg/mL"}], "application_number": "ANDA040541", "marketing_category": "ANDA", "marketing_start_date": "20210718", "listing_expiration_date": "20261231"}