propofol
Generic: propofol
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
propofol
Generic Name
propofol
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
INJECTION, EMULSION
Routes
Active Ingredients
propofol 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1470
Product ID
51662-1470_2b39ae97-5968-1329-e063-6294a90a2259
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077908
Listing Expiration
2026-12-31
Marketing Start
2019-12-14
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621470
Hyphenated Format
51662-1470
Supplemental Identifiers
RxCUI
UNII
NUI
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
propofol (source: ndc)
Generic Name
propofol (source: ndc)
Application Number
ANDA077908 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 100 mL in 1 VIAL (51662-1470-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "2b39ae97-5968-1329-e063-6294a90a2259", "openfda": {"nui": ["N0000175975", "N0000175681"], "unii": ["YI7VU623SF"], "rxcui": ["1808217"], "spl_set_id": ["99af9e0a-c268-84ca-e053-2a95a90a0a3e"], "pharm_class_pe": ["General Anesthesia [PE]"], "pharm_class_epc": ["General Anesthetic [EPC]"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 VIAL (51662-1470-1)", "package_ndc": "51662-1470-1", "marketing_start_date": "20191214"}], "brand_name": "PROPOFOL", "product_id": "51662-1470_2b39ae97-5968-1329-e063-6294a90a2259", "dosage_form": "INJECTION, EMULSION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "51662-1470", "generic_name": "PROPOFOL", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROPOFOL", "active_ingredients": [{"name": "PROPOFOL", "strength": "10 mg/mL"}], "application_number": "ANDA077908", "marketing_category": "ANDA", "marketing_start_date": "20191214", "listing_expiration_date": "20261231"}