propofol

Generic: propofol

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

Drug Facts

Product Profile

Brand Name propofol
Generic Name propofol
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION, EMULSION
Routes
INTRAVENOUS
Active Ingredients

propofol 10 mg/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

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)
general anesthetic [epc]
Physiologic Effect
general anesthesia [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621470
Hyphenated Format 51662-1470

Supplemental Identifiers

RxCUI
1808217
UNII
YI7VU623SF
NUI
N0000175975 N0000175681

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
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 100 mL in 1 VIAL (51662-1470-1)
source: ndc

Packages (1)

Ingredients (1)

propofol (10 mg/mL)

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"}