What is NDC 72572-612?

72572-612 is the product NDC for Propofol, Propofol 10 mg/mL injection, emulsion, listed with the FDA by Civica, Inc. It has 1 package NDC, shown above in 10- and 11-digit form.

Civica, Inc, NDC labeler code 72572. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Propofol?

29 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Propofol NDC 72572-612 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72572-612Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72572-0612Add 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
72572-612-10	7257206121072572061210	10 VIAL in 1 CARTON (72572-612-10) / 100 mL in 1 VIAL (72572-612-01)Marketed from Jul 16, 2021

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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: Civica, IncNDC labeler code 72572
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 205576
Marketing start: Jul 16, 2021
Listing expires: Dec 31, 2027
Other FDA classes: General Anesthesia (Physiologic effect)
Identifiers: Product ID 72572-612_8ae38e12-07f3-4a52-bbf8-36f6f49ccaf8SPL ID 8ae38e12-07f3-4a52-bbf8-36f6f49ccaf8SPL set ID 9ba70032-40c2-41c5-9f99-d1f94032d3dcRxCUI 1808217, 1808222, 1808224UNII YI7VU623SF
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

N472572061210 followed by a unit qualifier and the quantity

Package 72572-0612-10. 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

Current FDA label (SPL), effective Sep 18, 2026.

Indications (excerpt from the label)

Propofol injectable emulsion is an intravenous general anesthetic and sedation drug indicated for: • Induction of General Anesthesia for Patients Greater than or Equal to 3 Years of Age • Maintenance of General Anesthesia for Patients Greater than or Equal to 2 Months of Age • Initiation and Maintenance of Monitored Anesthesia Care (MAC) Sedation in Adult Patients • Sedation for Adult Patients in Combination with Regional Anesthesia • Intensive Care Unit (ICU) Sedation of Intubated, Mechanically Ventilated Adult Patients Limitations of Use Propofol injectable emulsion is not recommended for induction of anesthesia below the age of 3 years or for maintenance of anesthesia below the age of 2 m…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72572-612

What is NDC 72572-612?: 72572-612 is the product NDC for Propofol, Propofol 10 mg/mL injection, emulsion, listed with the FDA by Civica, Inc. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Propofol.
What is the active ingredient?: Propofol.
Who is the labeler?: Civica, Inc, NDC labeler code 72572. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Propofol?: 29 other product NDCs are listed under this name. See all Propofol NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Propofol NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Propofol	Propofol 10 mg/mL	Injection, EmulsionIntravenous	Hospira, Inc.	0409-0010	00409-0010-98
Propofol	Propofol 10 mg/mL	Injection, EmulsionIntravenous	Hospira, Inc.	0409-0501	00409-0501-98
Propofol	Propofol 10 mg/mL	Injection, EmulsionIntravenous	Hospira, Inc.	0409-1511	00409-1511-98
Propofol	Propofol 10 mg/mL	Injection, EmulsionIntravenous	Anthea Pharma Private Limited	83854-018	83854-0018-1083854-0018-1483854-0018-15+1 more
propofol	Propofol 10 mg/mL	Injection, EmulsionIntravenous	Meitheal Pharmaceuticals Inc.	71288-729	71288-0729-21
propofol	Propofol 10 mg/mL	Injection, EmulsionIntravenous	Meitheal Pharmaceuticals Inc.	71288-730	71288-0730-51
propofol	Propofol 10 mg/mL	Injection, EmulsionIntravenous	Meitheal Pharmaceuticals Inc.	71288-731	71288-0731-53
Propofol	Propofol 10 mg/mL	Injection, EmulsionIntravenous	Avenacy, LLC	83634-603	83634-0603-2083634-0603-5083634-0603-51
Propofol	Propofol 10 mg/mL	Injection, EmulsionIntravenous	Amneal Pharmaceuticals Private Limited	80830-1188	80830-1188-07
Propofol	Propofol 10 mg/mL	Injection, EmulsionIntravenous	Amneal Pharmaceuticals Private Limited	80830-2364	80830-2364-08

All 30 Propofol NDCs

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	Pfizer Laboratories Div Pfizer Inc	0069-0209
Propofol	Propofol 10 mg/mL	Injection, EmulsionIntravenous	Pfizer Laboratories Div Pfizer Inc	0069-0234
Propofol	Propofol 10 mg/mL	Injection, EmulsionIntravenous	Pfizer Laboratories Div Pfizer Inc	0069-0248
Propofol	Propofol 10 mg/mL	Injection, EmulsionIntravenous	Civica, Inc	72572-590
Propofol	Propofol 10 mg/mL	Injection, EmulsionIntravenous	Civica, Inc	72572-601