Prescription drug · ANDA
Cetrorelix Acetate NDC 71288-558
Kit · Subcutaneous · Meitheal Pharmaceuticals Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71288-558-90 | 7128805589071288055890 | 1 KIT in 1 CARTON (71288-558-90) * 2 mL in 1 VIAL, SINGLE-DOSE (71288-556-02) * 1 mL in 1 SYRINGE, GLASS (71288-557-81)Marketed from Apr 24, 2024 |
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)
- Cetrorelix Acetate
- Generic name (nonproprietary)
- cetrorelix acetate
- Dosage form
- Kit
- Route
- Subcutaneous
- Labeler
- Meitheal Pharmaceuticals Inc.NDC labeler code 71288
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 214540
- Marketing start
- Marketing end
- Identifiers
- Product ID 71288-558_3800c860-89c7-46fc-a58a-3cc5d96d2994SPL ID 3800c860-89c7-46fc-a58a-3cc5d96d2994
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
N471288055890followed by a unit qualifier and the quantityPackage 71288-0558-90. 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 71288-558
- What is NDC 71288-558?
- 71288-558 is the product NDC for Cetrorelix Acetate kit, 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?
- Cetrorelix Acetate.
- 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 Cetrorelix Acetate?
- 4 other product NDCs are listed under this name. See all Cetrorelix Acetate NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Cetrorelix Acetate products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| cetrorelix acetate | — | Kit | FRESENIUS KABI USA, LLC | 65219-292 | 65219-0292-77 |
| Cetrorelix acetatecetrorelix acetate for injection | — | KitSubcutaneous | Apotex Corp. | 60505-6270 | 60505-6270-01 |
| cetrorelix acetate | — | Kit | Gland Pharma Limited | 68083-600 | 68083-0600-01 |
| Cetrorelix acetatecetrorelix acetate for injection | — | KitSubcutaneous | Qilu Pharmaceutical Co., Ltd. | 67184-0605 | 67184-0605-02 |