Prescription drug · UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Teglutik (riluzole) NDC 70726-0304
Riluzole 5 mg/mL · Liquid · Oral · EDW PHARMA, INC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70726-0304-1 | 70726030401 | 300 mL in 1 BOTTLE, PLASTIC (70726-0304-1)Marketed from Jan 19, 2024 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
- Teglutik
- Generic name (nonproprietary)
- riluzole
- Active ingredients
- Riluzole — 5 mg/mL
- Dosage form
- Liquid
- Route
- Oral
- Labeler
- EDW PHARMA, INC
- Product type
- Prescription drug
- Marketing category
- Unapproved drug for use in drug shortage
- Marketing start
- Listing expires
- Other FDA classes
- Benzothiazoles (Chemical structure)
- Identifiers
- Product ID 70726-0304_4746bd79-5116-423c-e063-6394a90a17e1SPL ID 4746bd79-5116-423c-e063-6394a90a17e1SPL set ID 0f2b5cfc-a23d-699a-e063-6394a90a67d1RxCUI 2058147, 2675565UNII 7LJ087RS6F
- Pharmacologic class
- Benzothiazole
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 HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N470726030401followed by a unit qualifier and the quantityPackage 70726-0304-01. 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 .