Prescription drug · ANDA
propofol NDC 23155-345
Propofol 10 mg/mL · Injection, Emulsion · Intravenous · Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 23155-345-41 | 2315503454123155034541 | 10 VIAL in 1 CARTON (23155-345-41) / 20 mL in 1 VIAL (23155-345-31)Marketed from Jun 2, 2025 | |
| 23155-345-42 | 2315503454223155034542 | 20 VIAL in 1 CARTON (23155-345-42) / 50 mL in 1 VIAL (23155-345-32)Marketed from Jun 2, 2025 | |
| 23155-345-43 | 2315503454323155034543 | 10 VIAL in 1 CARTON (23155-345-43) / 100 mL in 1 VIAL (23155-345-33)Marketed from Jun 2, 2025 | |
| 23155-345-44 | 2315503454423155034544 | 20 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
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.NDC labeler code 23155
- 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.
- NDC on a medical claim
N423155034541followed by a unit qualifier and the quantityPackage 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.
Related NDCs: other propofol products
Other finished products listed under the same name: strengths, forms and labelers.
| 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 |
Other NDCs under ANDA 206408
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| propofol | Propofol 10 mg/mL | Injection, EmulsionIntravenous | NorthStar Rx LLC | 16714-528 |
| propofol | Propofol 10 mg/mL | Injection, EmulsionIntravenous | NorthStar Rx LLC | 16714-690 |
| propofol | Propofol 10 mg/mL | Injection, EmulsionIntravenous | NorthStar Rx LLC | 16714-977 |
| Propofol | Propofol 10 mg/mL | Injection, EmulsionIntravenous | Avenacy, LLC | 83634-603 |