NDC codes

FDA NDC Directory
Product NDC (as listed)68071-4562Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-4562Add 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
68071-4562-968071456209680714562099 TABLET in 1 BOX (68071-4562-9)Marketed from Sep 18, 2018

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)
Sumatriptan Succinate
Generic name (nonproprietary)
sumatriptan succinate
Active ingredients
Sumatriptan succinate — 50 mg/1
Dosage form
Tablet
Route
Oral
Labeler
NuCare Pharmaceuticals,Inc.NDC labeler code 68071
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 68071-4562_2b36bbed-fb22-3b1f-e063-6294a90ac2deSPL ID 2b36bbed-fb22-3b1f-e063-6294a90ac2deSPL set ID 7628caf4-5272-4e42-e053-2a91aa0a2f24RxCUI 313161UNII J8BDZ68989UPC 0368071456295
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

N468071456209 followed by a unit qualifier and the quantity

Package 68071-4562-09. 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)

About NDC 68071-4562

What is NDC 68071-4562?
68071-4562 is the product NDC for Sumatriptan Succinate, Sumatriptan succinate 50 mg/1 tablet, listed with the FDA by NuCare Pharmaceuticals,Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Sumatriptan Succinate.
What is the active ingredient?
Sumatriptan succinate.
Who is the labeler?
NuCare Pharmaceuticals,Inc., NDC labeler code 68071. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Sumatriptan Succinate?
32 other product NDCs are listed under this name. See all Sumatriptan 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 Sumatriptan Succinate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Sumatriptan SuccinateSumatriptan succinate 4 mg/.5mLInjectionSubcutaneousAlembic Pharmaceuticals Limited46708-65646708-0656-0146708-0656-05
Sumatriptan SuccinateSumatriptan succinate 6 mg/.5mLInjectionSubcutaneousAlembic Pharmaceuticals Limited46708-65746708-0657-0146708-0657-05
Sumatriptan SuccinateSumatriptan succinate 4 mg/.5mLInjectionSubcutaneousAlembic Pharmaceuticals Inc.62332-65662332-0656-0162332-0656-05
Sumatriptan SuccinateSumatriptan succinate 6 mg/.5mLInjectionSubcutaneousAlembic Pharmaceuticals Inc.62332-65762332-0657-0162332-0657-05
Sumatriptan SuccinateSumatriptan succinate 6 mg/.5mLInjectionSubcutaneousSun Pharmaceutical Industries, Inc.47335-27647335-0276-4047335-0276-41
Sumatriptan SuccinateSumatriptan succinate 25 mg/1Tablet, Film coatedOralDirect_Rx72189-59672189-0596-09
Sumatriptan SuccinateSumatriptan succinate 6 mg/.5mLInjectionSubcutaneousNorthStar Rx LLC72603-14172603-0141-02
Sumatriptan SuccinateSumatriptan succinate 6 mg/.5mLInjectionSubcutaneousDr. Reddys Laboratories Inc.,43598-76843598-0768-23
Sumatriptan SuccinateSumatriptan succinate 6 mg/.5mLInjectionSubcutaneousSportpharm LLC85766-23885766-0238-02
Sumatriptan SuccinateSumatriptan succinate 25 mg/1Tablet, Film coatedOralDirect_Rx72189-43272189-0432-09

All 33 Sumatriptan Succinate NDCs

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/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/1TabletOralProficient Rx LP63187-049
Sumatriptan SuccinateSumatriptan succinate 100 mg/1TabletOralProficient Rx LP63187-607
Sumatriptan SuccinateSumatriptan succinate 25 mg/1TabletOralProficient Rx LP63187-617
Sumatriptan SuccinateSumatriptan succinate 100 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-2283
Sumatriptan SuccinateSumatriptan succinate 50 mg/1TabletOralAsclemed USA, Inc.76420-093

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