propofol
Generic: propofol
Labeler: pfizer laboratories div pfizer incDrug Facts
Product Profile
Brand Name
propofol
Generic Name
propofol
Labeler
pfizer laboratories div pfizer inc
Dosage Form
INJECTION, EMULSION
Routes
Active Ingredients
propofol 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0069-0248
Product ID
0069-0248_c56a182a-6142-428f-9ac0-0f4dce23af7f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205576
Listing Expiration
2026-12-31
Marketing Start
2020-10-05
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00690248
Hyphenated Format
0069-0248
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
ANDA205576 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 10 VIAL in 1 CARTON (0069-0248-10) / 100 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "c56a182a-6142-428f-9ac0-0f4dce23af7f", "openfda": {"nui": ["N0000175975", "N0000175681"], "unii": ["YI7VU623SF"], "rxcui": ["1808217", "1808222", "1808224"], "spl_set_id": ["3acf8e6c-827d-11e2-9e96-0800200c9a66"], "pharm_class_pe": ["General Anesthesia [PE]"], "pharm_class_epc": ["General Anesthetic [EPC]"], "manufacturer_name": ["Pfizer Laboratories Div Pfizer Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (0069-0248-10) / 100 mL in 1 VIAL", "package_ndc": "0069-0248-10", "marketing_start_date": "20201005"}], "brand_name": "Propofol", "product_id": "0069-0248_c56a182a-6142-428f-9ac0-0f4dce23af7f", "dosage_form": "INJECTION, EMULSION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "0069-0248", "generic_name": "Propofol", "labeler_name": "Pfizer Laboratories Div Pfizer Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propofol", "active_ingredients": [{"name": "PROPOFOL", "strength": "10 mg/mL"}], "application_number": "ANDA205576", "marketing_category": "ANDA", "marketing_start_date": "20201005", "listing_expiration_date": "20261231"}