NDC codes

FDA NDC Directory
Product NDC (as listed)23155-345Labeler and product segments. Claims need a package NDC.
Product NDC at billing width23155-0345Add 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 NDC11-digit (billing)PackageCopy
23155-345-41231550345412315503454110 VIAL in 1 CARTON (23155-345-41) / 20 mL in 1 VIAL (23155-345-31)Marketed from Jun 2, 2025
23155-345-42231550345422315503454220 VIAL in 1 CARTON (23155-345-42) / 50 mL in 1 VIAL (23155-345-32)Marketed from Jun 2, 2025
23155-345-43231550345432315503454310 VIAL in 1 CARTON (23155-345-43) / 100 mL in 1 VIAL (23155-345-33)Marketed from Jun 2, 2025
23155-345-44231550345442315503454420 VIAL in 1 CARTON (23155-345-44) / 20 mL in 1 VIAL (23155-345-31)Marketed from Jun 2, 2025

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
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 206408
Marketing start
Listing expires
Other FDA classes
General Anesthesia (Physiologic effect)
Identifiers
Product ID 23155-345_f31234b2-af75-4abd-9d5d-fc8a754e8725SPL ID f31234b2-af75-4abd-9d5d-fc8a754e8725
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

N423155034541 followed by a unit qualifier and the quantity

Package 23155-0345-41. 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.

About NDC 23155-345

What is NDC 23155-345?
23155-345 is the product NDC for propofol, Propofol 10 mg/mL injection, emulsion, listed with the FDA by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.. It has 4 package NDCs, 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?
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc., NDC labeler code 23155. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
PropofolPropofol 10 mg/mLInjection, EmulsionIntravenousHospira, Inc.0409-001000409-0010-98
PropofolPropofol 10 mg/mLInjection, EmulsionIntravenousHospira, Inc.0409-050100409-0501-98
PropofolPropofol 10 mg/mLInjection, EmulsionIntravenousHospira, Inc.0409-151100409-1511-98
PropofolPropofol 10 mg/mLInjection, EmulsionIntravenousAnthea Pharma Private Limited83854-01883854-0018-1083854-0018-1483854-0018-15+1 more
propofolPropofol 10 mg/mLInjection, EmulsionIntravenousMeitheal Pharmaceuticals Inc.71288-72971288-0729-21
propofolPropofol 10 mg/mLInjection, EmulsionIntravenousMeitheal Pharmaceuticals Inc.71288-73071288-0730-51
propofolPropofol 10 mg/mLInjection, EmulsionIntravenousMeitheal Pharmaceuticals Inc.71288-73171288-0731-53
PropofolPropofol 10 mg/mLInjection, EmulsionIntravenousAvenacy, LLC83634-60383634-0603-2083634-0603-5083634-0603-51
PropofolPropofol 10 mg/mLInjection, EmulsionIntravenousAmneal Pharmaceuticals Private Limited80830-118880830-1188-07
PropofolPropofol 10 mg/mLInjection, EmulsionIntravenousAmneal Pharmaceuticals Private Limited80830-236480830-2364-08

All 30 propofol NDCs

Other NDCs under ANDA 206408

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

FDA NDC Directory listings under ANDA 206408
ProductStrengthForm · routeLabelerProduct NDC
propofolPropofol 10 mg/mLInjection, EmulsionIntravenousNorthStar Rx LLC16714-528
propofolPropofol 10 mg/mLInjection, EmulsionIntravenousNorthStar Rx LLC16714-690
propofolPropofol 10 mg/mLInjection, EmulsionIntravenousNorthStar Rx LLC16714-977
PropofolPropofol 10 mg/mLInjection, EmulsionIntravenousAvenacy, LLC83634-603

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