Propofol NDC 0069-0234

NDC codes

FDA NDC Directory

Product NDC (as listed)0069-0234Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00069-0234Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
0069-0234-20	00069023420	20 VIAL in 1 CARTON (0069-0234-20) / 50 mL in 1 VIALMarketed from Oct 5, 2020

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Propofol
Generic name (nonproprietary): propofol
Active ingredients: Propofol — 10 mg/mL
Dosage form: Injection, Emulsion
Route: Intravenous
Labeler: Pfizer Laboratories Div Pfizer Inc
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 205576
Marketing start: Oct 5, 2020
Listing expires: Dec 31, 2027
Other FDA classes: General Anesthesia (Physiologic effect)
Identifiers: Product ID 0069-0234_5701fd0d-b178-4d52-a6c5-ba78f74d645cSPL ID 5701fd0d-b178-4d52-a6c5-ba78f74d645c
Pharmacologic class: General Anesthetic

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N400069023420 followed by a unit qualifier and the quantity

Package 00069-0234-20. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 205576

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 205576
Product	Strength	Form · route	Labeler	Product NDC
Propofol	Propofol 10 mg/mL	Injection, EmulsionIntravenous	Civica, Inc	72572-590
Propofol	Propofol 10 mg/mL	Injection, EmulsionIntravenous	Civica, Inc	72572-601
Propofol	Propofol 10 mg/mL	Injection, EmulsionIntravenous	Civica, Inc	72572-612
Propofol	Propofol 10 mg/mL	Injection, EmulsionIntravenous	Pfizer Laboratories Div Pfizer Inc	0069-0248
Propofol	Propofol 10 mg/mL	Injection, EmulsionIntravenous	Pfizer Laboratories Div Pfizer Inc	0069-0209