propofol

Generic: propofol

Labeler: sagent pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propofol
Generic Name propofol
Labeler sagent pharmaceuticals
Dosage Form INJECTION, EMULSION
Routes
INTRAVENOUS
Active Ingredients

propofol 10 mg/mL

Manufacturer
Sagent Pharmaceuticals

Identifiers & Regulatory

Product NDC 25021-608
Product ID 25021-608_24f96546-ad32-43ca-be91-5536e26d4137
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075102
Listing Expiration 2026-12-31
Marketing Start 2014-07-01

Pharmacologic Class

Established (EPC)
general anesthetic [epc]
Physiologic Effect
general anesthesia [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 25021608
Hyphenated Format 25021-608

Supplemental Identifiers

RxCUI
1808217 1808222 1808224
UNII
YI7VU623SF
NUI
N0000175975 N0000175681

Packaging Origin

Original Packager
true

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 ANDA075102 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (25021-608-20) / 20 mL in 1 VIAL
  • 20 VIAL in 1 CARTON (25021-608-50) / 50 mL in 1 VIAL
  • 10 VIAL in 1 CARTON (25021-608-51) / 100 mL in 1 VIAL
source: ndc

Packages (3)

25021-608-20 25 VIAL in 1 CARTON (25021-608-20) / 20 mL in 1 VIAL 25021-608-50 20 VIAL in 1 CARTON (25021-608-50) / 50 mL in 1 VIAL 25021-608-51 10 VIAL in 1 CARTON (25021-608-51) / 100 mL in 1 VIAL

Ingredients (1)

propofol (10 mg/mL)

Linked Drug Pages (1)

propofol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "24f96546-ad32-43ca-be91-5536e26d4137", "openfda": {"nui": ["N0000175975", "N0000175681"], "unii": ["YI7VU623SF"], "rxcui": ["1808217", "1808222", "1808224"], "spl_set_id": ["fa93f173-7858-4d88-860e-76ab97e65c2f"], "pharm_class_pe": ["General Anesthesia [PE]"], "pharm_class_epc": ["General Anesthetic [EPC]"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (25021-608-20)  / 20 mL in 1 VIAL", "package_ndc": "25021-608-20", "marketing_start_date": "20140701"}, {"sample": false, "description": "20 VIAL in 1 CARTON (25021-608-50)  / 50 mL in 1 VIAL", "package_ndc": "25021-608-50", "marketing_start_date": "20140701"}, {"sample": false, "description": "10 VIAL in 1 CARTON (25021-608-51)  / 100 mL in 1 VIAL", "package_ndc": "25021-608-51", "marketing_start_date": "20140701"}], "brand_name": "propofol", "product_id": "25021-608_24f96546-ad32-43ca-be91-5536e26d4137", "dosage_form": "INJECTION, EMULSION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "25021-608", "generic_name": "propofol", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "propofol", "active_ingredients": [{"name": "PROPOFOL", "strength": "10 mg/mL"}], "application_number": "ANDA075102", "marketing_category": "ANDA", "marketing_start_date": "20140701", "listing_expiration_date": "20261231"}