NDC codes

FDA NDC Directory
Product NDC (as listed)63187-607Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63187-0607Add 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
63187-607-09631870607099 BLISTER PACK in 1 CARTON (63187-607-09) / 9 TABLET in 1 BLISTER PACKMarketed from Dec 1, 2018

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)
Sumatriptan Succinate
Generic name (nonproprietary)
sumatriptan succinate
Active ingredients
Sumatriptan succinate — 100 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076847
Marketing start
Listing expires
Other FDA classes
Serotonin 1b Receptor Agonists (Mechanism)Serotonin 1d Receptor Agonists (Mechanism)
Identifiers
Product ID 63187-607_11962982-e9c2-4dca-a018-1573c6b43ad8SPL ID 11962982-e9c2-4dca-a018-1573c6b43ad8SPL set ID d9c78ac5-7328-4204-8f66-96606d7db5c3RxCUI 313160UNII J8BDZ68989
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

N463187060709 followed by a unit qualifier and the quantity

Package 63187-0607-09. 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)

INDICATIONS AND USAGE Sumatriptan tablets are indicated for the acute treatment of migraine attacks with or without aura in adults. Sumatriptan tablets are not intended for the prophylactic therapy of migraine or for use in the management of hemiplegic or basilar migraine (see CONTRAINDICATIONS ). Safety and effectiveness of sumatriptan tablets have not been established for cluster headache, which is present in an older, predominantly male population.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 076847

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

FDA NDC Directory listings under ANDA 076847
ProductStrengthForm · routeLabelerProduct NDC
Sumatriptan SuccinateSumatriptan succinate 25 mg/1TabletOralProficient Rx LP63187-617
Sumatriptan SuccinateSumatriptan succinate 50 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4562
Sumatriptan SuccinateSumatriptan succinate 100 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-2283
Sumatriptan SuccinateSumatriptan succinate 25 mg/1TabletOralDr. Reddy's Laboratories Limited55111-291
Sumatriptan SuccinateSumatriptan succinate 50 mg/1TabletOralDr. Reddy's Laboratories Limited55111-292
Sumatriptan SuccinateSumatriptan succinate 100 mg/1TabletOralDr. Reddy's Laboratories Limited55111-293
Sumatriptan SuccinateSumatriptan succinate 50 mg/1TabletOralAsclemed USA, Inc.76420-093
Sumatriptan SuccinateSumatriptan succinate 50 mg/1TabletOralProficient Rx LP63187-049

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