NDC codes

FDA NDC Directory
Product NDC (as listed)69315-157Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69315-0157Add 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
69315-157-13693150157139 TABLET, FILM COATED in 1 CARTON (69315-157-13)Marketed from Feb 28, 2026

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)
Frovatriptan Succinate
Generic name (nonproprietary)
frovatriptan succinate
Active ingredients
Frovatriptan succinate — 2.5 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Leading Pharma, LLCNDC labeler code 69315
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 216998
Marketing start
Listing expires
Other FDA classes
Serotonin 1b Receptor Agonists (Mechanism)Serotonin 1d Receptor Agonists (Mechanism)
Identifiers
Product ID 69315-157_88509316-ddfb-4995-8251-c0b39f4e8aacSPL ID 88509316-ddfb-4995-8251-c0b39f4e8aacSPL set ID d303af88-e0c1-4fb2-ba8e-83b7e6d163cdRxCUI 349462UNII D28J6W18HY
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

N469315015713 followed by a unit qualifier and the quantity

Package 69315-0157-13. 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)

Frovatriptan succinate tablets are indicated for the acute treatment of migraine with or without aura in adults. Limitations of Use Use only if a clear diagnosis of migraine has been established. If a patient has no response for the first migraine attack treated with frovatriptan succinate tablets, reconsider the diagnosis of migraine before frovatriptan succinate tablets are administered to treat any subsequent attacks. Frovatriptan succinate tablets are not indicated for the prevention of migraine attacks. Safety and effectiveness of frovatriptan succinate tablets have not been established for cluster headache. Frovatriptan succinate is a serotonin (5-HT 1 B/1D ) receptor agonist (triptan)…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 69315-157

What is NDC 69315-157?
69315-157 is the product NDC for Frovatriptan Succinate, Frovatriptan succinate 2.5 mg/1 tablet, film coated, listed with the FDA by Leading Pharma, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Frovatriptan Succinate.
What is the active ingredient?
Frovatriptan succinate.
Who is the labeler?
Leading Pharma, LLC, NDC labeler code 69315. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Frovatriptan Succinate?
1 other product NDC are listed under this name. See all Frovatriptan Succinate NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Frovatriptan Succinate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
frovatriptan succinateFrovatriptan succinate 2.5 mg/1Tablet, Film coatedOralGlenmark Pharmaceuticals Inc., USA68462-69468462-0694-97

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