NDC codes

FDA NDC Directory
Product NDC (as listed)50090-8038Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-8038Add 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 NDC11-digit (billing)PackageCopy
50090-8038-0500908038003 FILM in 1 BOTTLE (50090-8038-0)Marketed from Aug 26, 2026
50090-8038-1500908038019 FILM in 1 BOTTLE (50090-8038-1)Marketed from Aug 26, 2026

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)
Rizafilm
Generic name (nonproprietary)
rizatriptan benzoate
Active ingredients
Rizatriptan benzoate — 10 mg/1
Dosage form
Film
Route
Oral
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 205394
Marketing start
Listing expires
Other FDA classes
Serotonin 1b Receptor Agonists (Mechanism)Serotonin 1d Receptor Agonists (Mechanism)
Identifiers
Product ID 50090-8038_07cd6b0a-291d-4a45-8f01-a2d68239623cSPL ID 07cd6b0a-291d-4a45-8f01-a2d68239623cSPL set ID 8e36b946-cf2a-44d9-9ba7-4385cfe6b360RxCUI 2634482, 2672955UNII WR978S7QHH
Pharmacologic class
Serotonin-1b and Serotonin-1d Receptor Agonist

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

N450090803800 followed by a unit qualifier and the quantity

Package 50090-8038-00. 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

RizaFilm™ is indicated for the acute treatment of migraine with or without aura in adults and in pediatric patients 6 to 17 years of age. Limitations of Use RizaFilm should only be used where a clear diagnosis of migraine has been established. If a patient has no response for the first migraine attack treated with RizaFilm, the diagnosis of migraine should be reconsidered before RizaFilm is administered to treat any subsequent attacks. RizaFilm is not indicated for the preventive treatment of migraine. Safety and effectiveness of RizaFilm have not been established for cluster headache. RizaFilm is a serotonin (5-HT) 1B/1D receptor agonist (triptan) indicated for the acute treatment of migrai…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under NDA 205394

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

FDA NDC Directory listings under NDA 205394
ProductStrengthForm · routeLabelerProduct NDC
Rizafilmrizatriptan benzoateRizatriptan benzoate 5 mg/1FilmOralGensco Laboratories LLC35781-0605
Rizafilmrizatriptan benzoateRizatriptan benzoate 10 mg/1FilmOralGensco Laboratories LLC35781-0600

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