Prescription drug · UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Teglutik (Riluzole) NDC 70726-0306
Riluzole 5 mg/mL · Liquid · Oral · EDW PHARMA
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70726-0306-1 | 70726030601 | 300 mL in 1 BOTTLE, PLASTIC (70726-0306-1)Marketed from Jun 10, 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 PHARMANDC labeler code 70726
- 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 70726-0306_4746bb53-bb35-7aa0-e063-6394a90a647bSPL ID 4746bb53-bb35-7aa0-e063-6394a90a647bSPL set ID 1a3aeb59-d589-8d12-e063-6394a90a0a3aRxCUI 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
N470726030601followed by a unit qualifier and the quantityPackage 70726-0306-01. 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 .
About NDC 70726-0306
- What is NDC 70726-0306?
- 70726-0306 is the product NDC for Teglutik (riluzole), Riluzole 5 mg/mL liquid, listed with the FDA by EDW PHARMA. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Teglutik (Riluzole).
- What is the active ingredient?
- Riluzole.
- Who is the labeler?
- EDW PHARMA, NDC labeler code 70726. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Teglutik?
- 2 other product NDCs are listed under this name. See all Teglutik NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Teglutik products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Teglutikriluzole | Riluzole 5 mg/mL | LiquidOral | EDW PHARMA | 70726-0305 | 70726-0305-01 |
| Teglutikriluzole | Riluzole 5 mg/mL | LiquidOral | EDW PHARMA, INC | 70726-0304 | 70726-0304-01 |