NDC codes

FDA NDC Directory
Product NDC (as listed)47335-276Labeler and product segments. Claims need a package NDC.
Product NDC at billing width47335-0276Add 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
47335-276-40473350276401 SYRINGE in 1 PACKAGE (47335-276-40) / .5 mL in 1 SYRINGEMarketed from Aug 20, 2025
47335-276-41473350276412 SYRINGE in 1 PACKAGE (47335-276-41) / .5 mL in 1 SYRINGEMarketed from Aug 20, 2025

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 — 6 mg/.5mL
Dosage form
Injection
Route
Subcutaneous
Labeler
Sun Pharmaceutical Industries, Inc.NDC labeler code 47335
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090358
Marketing start
Listing expires
Other FDA classes
Serotonin 1b Receptor Agonists (Mechanism)Serotonin 1d Receptor Agonists (Mechanism)
Identifiers
Product ID 47335-276_2642fcb9-4170-4b4c-818b-74c071cb567eSPL ID 2642fcb9-4170-4b4c-818b-74c071cb567eSPL set ID f235152e-dd8d-4679-9d9f-404fe5ff4fbaRxCUI 1657151UNII 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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N447335027640 followed by a unit qualifier and the quantity

Package 47335-0276-40. 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)

Sumatriptan injection is indicated in adults for (1) the acute treatment of migraine, with or without aura, and (2) the acute treatment of cluster headache. Limitations of Use Use only if a clear diagnosis of migraine or cluster headache has been established. If a patient has no response to the first migraine or cluster headache attack treated with sumatriptan injection, reconsider the diagnosis before sumatriptan injection is administered to treat any subsequent attacks. Sumatriptan injection is not indicated for the prevention of migraine or cluster headache attacks. Sumatriptan is a serotonin (5-HT 1B/1D ) receptor agonist (triptan) indicated for: Acute treatment of migraine with or witho…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 47335-276

What is NDC 47335-276?
47335-276 is the product NDC for Sumatriptan Succinate, Sumatriptan succinate 6 mg/.5mL injection, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 2 package NDCs, 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?
Sun Pharmaceutical Industries, Inc., NDC labeler code 47335. 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?
34 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 Inc.62332-65662332-0656-0162332-0656-05
Sumatriptan SuccinateSumatriptan succinate 6 mg/.5mLInjectionSubcutaneousAlembic Pharmaceuticals Inc.62332-65762332-0657-0162332-0657-05
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 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
Sumatriptan SuccinateSumatriptan succinate 50 mg/1Tablet, Film coatedOralDirect_Rx72189-43372189-0433-09

All 35 Sumatriptan Succinate NDCs

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