NDC 63629-8188

Sumatriptan

Sumatriptan Succinate

Sumatriptan is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Sumatriptan Succinate.

Product ID63629-8188_cdaec209-ee16-4071-8f9f-5a534410afe2
NDC63629-8188
Product TypeHuman Prescription Drug
Proprietary NameSumatriptan
Generic NameSumatriptan Succinate
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2009-08-17
Marketing CategoryANDA / ANDA
Application NumberANDA078327
Labeler NameBryant Ranch Prepack
Substance NameSUMATRIPTAN SUCCINATE
Active Ingredient Strength100 mg/1
Pharm ClassesSerotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC],Serotonin 1b Receptor Agonists [MoA]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 63629-8188-1

9 TABLET in 1 BOTTLE (63629-8188-1)
Marketing Start Date2019-08-02
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63629-8188-1 [63629818801]

Sumatriptan TABLET
Marketing CategoryANDA
Application NumberANDA078327
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-08-02

Drug Details

Active Ingredients

IngredientStrength
SUMATRIPTAN SUCCINATE100 mg/1

OpenFDA Data

SPL SET ID:a6a4e17a-7841-43cb-b435-e4eb11105a80
Manufacturer
UNII

Pharmacological Class

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

NDC Crossover Matching brand name "Sumatriptan" or generic name "Sumatriptan Succinate"

NDCBrand NameGeneric Name
0093-2013Sumatriptansumatriptan succinate
0093-2014Sumatriptansumatriptan succinate
0143-9638SUMATRIPTANsumatriptan
68071-3350SumatriptanSumatriptan
68071-4061SumatriptanSumatriptan
68071-4815SumatriptanSumatriptan
68788-6769SumatriptanSumatriptan
68788-6778SumatriptanSumatriptan
68788-9547SumatriptanSumatriptan
0527-1818SumatriptanSumatriptan
0527-1859SumatriptanSumatriptan
70518-0041SumatriptanSumatriptan
70518-1184SumatriptanSumatriptan
0781-6523SUMATRIPTANSUMATRIPTAN
0781-6524SUMATRIPTANSUMATRIPTAN
16714-796SumatriptanSumatriptan
16714-532SumatriptanSumatriptan
16714-533SumatriptanSumatriptan
16714-798SumatriptanSumatriptan
16714-531SumatriptanSumatriptan
16714-797SumatriptanSumatriptan
25021-703sumatriptansumatriptan
33261-663SumatriptanSumatriptan
50090-2053sumatriptansumatriptan
50090-2144SumatriptanSumatriptan
50090-1129SumatriptanSumatriptan
50090-1130SumatriptanSumatriptan
50090-2497SUMATRIPTANSUMATRIPTAN
50436-0147SumatriptanSumatriptan
50436-4623SUMATRIPTANSUMATRIPTAN
50436-4622SUMATRIPTANSUMATRIPTAN
53002-2592SumatriptanSumatriptan
53002-1562SumatriptanSumatriptan
53002-2593SumatriptanSumatriptan
55150-173SumatriptanSumatriptan
60429-994SumatriptanSumatriptan
60429-995SUMATRIPTANSUMATRIPTAN
61919-300SUMATRIPTANSUMATRIPTAN
63187-931SumatriptanSumatriptan
63187-164SUMATRIPTANSUMATRIPTAN
63304-097SUMATRIPTANSUMATRIPTAN
63187-323SUMATRIPTANSUMATRIPTAN
63187-797SumatriptanSumatriptan
63304-098SUMATRIPTANSUMATRIPTAN
63187-969SumatriptanSumatriptan
63304-099SUMATRIPTANSUMATRIPTAN
65862-146SumatriptanSumatriptan
65862-147SumatriptanSumatriptan
0173-0449IMITREXsumatriptan
0173-0478IMITREXsumatriptan

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.