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sumatriptan succinate

NDC 62756-520, sumatriptan succinate, tablet, film coated, from Sun Pharmaceutical Industries, Inc..

Product NDC
62756-520
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078295
DEA schedule
None
Request
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Product

Active ingredients and packages

Active ingredients

  • SUMATRIPTAN SUCCINATE25 mg/1

Pharmacologic classes

Serotonin 1b Receptor Agonists [MoA]; Serotonin 1d Receptor Agonists [MoA]; Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]

Package NDCNDC-11Package
62756-520-01627560520013 BLISTER PACK in 1 CARTON (62756-520-01) / 9 TABLET, FILM COATED in 1 BLISTER PACK
62756-520-0862756052008100 TABLET, FILM COATED in 1 BOTTLE (62756-520-08)
62756-520-18627560520181000 TABLET, FILM COATED in 1 BOTTLE (62756-520-18)
62756-520-836275605208330 TABLET, FILM COATED in 1 BOTTLE (62756-520-83)
62756-520-93627560520939 BLISTER PACK in 1 CARTON (62756-520-93) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

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curl
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.