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Sumatriptan - Medication Information

Product NDC Code 68071-5072
Drug Name

Sumatriptan

Type Brand
Pharm Class Serotonin 1b Receptor Agonists [MoA],
Serotonin 1d Receptor Agonists [MoA],
Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]
Active Ingredients
Sumatriptan succinate 100 mg/1
Route ORAL
Dosage Form TABLET
RxCUI drug identifier 313160
Application Number ANDA078327
Labeler Name NuCare Pharmaceuticals,Inc.
Packages
Package NDC Code Description
68071-5072-9 9 tablet in 1 box (68071-5072-9)
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Spl product data elements

Usually a list of ingredients in a drug product.
Sumatriptan Sumatriptan Succinate CROSCARMELLOSE SODIUM CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE POLYSORBATE 80 SODIUM BICARBONATE SUMATRIPTAN SUCCINATE SUMATRIPTAN White to off-white biconvex C;34

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - pdp

Spl medguide

Information about the patient medication guide that accompanies the drug product. Certain drugs must be dispensed with an accompanying medication guide. This field may contain information about when to consult the medication guide and the contents of the medication guide.
Sumatriptan Succinate Tablets

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API