Prescription drug · UNAPPROVED DRUG OTHER
Fluopar NDC 59088-754
fluocinonide, dimethicone · Kit · PureTek Corporation
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 59088-754-00 | 59088075400 | 1 KIT in 1 KIT (59088-754-00) * 1 TUBE in 1 CARTON (45802-151-94) / 30 g in 1 TUBE * 118 mL in 1 TUBE (59088-333-08)Marketed from Mar 3, 2020 |
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)
- Fluopar
- Generic name (nonproprietary)
- fluocinonide, dimethicone
- Dosage form
- Kit
- Labeler
- PureTek Corporation
- Product type
- Prescription drug
- Marketing category
- Unapproved drug (other)
- Marketing start
- Listing expires
- Identifiers
- Product ID 59088-754_292ff5ee-68a5-7a8c-e063-6294a90a29e4SPL ID 292ff5ee-68a5-7a8c-e063-6294a90a29e4SPL set ID 9ff7fa78-0fca-976f-e053-2995a90a4641RxCUI 259090, 485647
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.
- NDC on a medical claim
N459088075400followed by a unit qualifier and the quantityPackage 59088-0754-00. 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
Label details couldn’t be retrieved right now. Open the label on DailyMed.