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Sumatriptan Succinate - 68788-9004-9 - (Sumatriptan Succinate)

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Drug Information of Sumatriptan Succinate

Product NDC: 68788-9004
Proprietary Name: Sumatriptan Succinate
Non Proprietary Name: Sumatriptan Succinate
Active Ingredient(s): 25    mg/1 & nbsp;   Sumatriptan Succinate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Sumatriptan Succinate

Product NDC: 68788-9004
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076847
Marketing Category: ANDA
Start Marketing Date: 20110608

Package Information of Sumatriptan Succinate

Package NDC: 68788-9004-9
Package Description: 9 BLISTER PACK in 1 CARTON (68788-9004-9) > 9 TABLET in 1 BLISTER PACK

NDC Information of Sumatriptan Succinate

NDC Code 68788-9004-9
Proprietary Name Sumatriptan Succinate
Package Description 9 BLISTER PACK in 1 CARTON (68788-9004-9) > 9 TABLET in 1 BLISTER PACK
Product NDC 68788-9004
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sumatriptan Succinate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110608
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name SUMATRIPTAN SUCCINATE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]

Complete Information of Sumatriptan Succinate


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