What is NDC 71288-730?

71288-730 is the product NDC for propofol, Propofol 10 mg/mL injection, emulsion, listed with the FDA by Meitheal Pharmaceuticals Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Meitheal Pharmaceuticals Inc., NDC labeler code 71288. 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 71288-730 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71288-730Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71288-0730Add 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
71288-730-51	7128807305171288073051	10 VIAL in 1 CARTON (71288-730-51) / 50 mL in 1 VIAL (71288-730-50)Marketed from Dec 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: Meitheal Pharmaceuticals Inc.NDC labeler code 71288
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217945
Marketing start: Dec 2, 2025
Listing expires: Dec 31, 2026
Other FDA classes: General Anesthesia (Physiologic effect)
Identifiers: Product ID 71288-730_98e25b4f-43c4-4269-8213-aacb02a75099SPL ID 98e25b4f-43c4-4269-8213-aacb02a75099SPL set ID 548d5192-2e5e-4c1b-8f17-940b6e791ae5RxCUI 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

N471288073051 followed by a unit qualifier and the quantity

Package 71288-0730-51. 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 Dec 12, 2025.

Indications (excerpt from the label)

• 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 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 …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71288-730

What is NDC 71288-730?: 71288-730 is the product NDC for propofol, Propofol 10 mg/mL injection, emulsion, listed with the FDA by Meitheal Pharmaceuticals 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?: Meitheal Pharmaceuticals Inc., NDC labeler code 71288. 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.	71288-731	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
Propofol	Propofol 10 mg/mL	Injection, EmulsionIntravenous	Amneal Pharmaceuticals Private Limited	80830-2365	80830-2365-07

All 30 propofol NDCs

Other NDCs under ANDA 217945

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

FDA NDC Directory listings under ANDA 217945
Product	Strength	Form · route	Labeler	Product NDC
propofol	Propofol 10 mg/mL	Injection, EmulsionIntravenous	Meitheal Pharmaceuticals Inc.	71288-729
propofol	Propofol 10 mg/mL	Injection, EmulsionIntravenous	Meitheal Pharmaceuticals Inc.	71288-731