NDC 71800-901

Sumatriptan and Naproxen Sodium

Sumatriptan And Naproxen Sodium

Sumatriptan and Naproxen Sodium is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Innovida Phamaceutique Corporation. The primary component is Sumatriptan Succinate; Naproxen Sodium.

Product ID71800-901_19d5024a-b131-41c3-8cee-5e20564154aa
NDC71800-901
Product TypeHuman Prescription Drug
Proprietary NameSumatriptan and Naproxen Sodium
Generic NameSumatriptan And Naproxen Sodium
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2020-12-09
Marketing CategoryANDA / ANDA
Application NumberANDA202803
Labeler NameInnovida Phamaceutique Corporation
Substance NameSUMATRIPTAN SUCCINATE; NAPROXEN SODIUM
Active Ingredient Strength85 mg/1; mg/1
Pharm ClassesSerotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC],Serotonin 1b Receptor Agonists [MoA],Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 71800-901-01

9 TABLET, FILM COATED in 1 BOTTLE (71800-901-01)
Marketing Start Date2020-12-09
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Sumatriptan and Naproxen Sodium" or generic name "Sumatriptan And Naproxen Sodium"

NDCBrand NameGeneric Name
0378-8755Sumatriptan and Naproxen Sodiumsumatriptan and naproxen sodium
16714-891Sumatriptan and Naproxen SodiumSumatriptan and Naproxen Sodium
47335-410Sumatriptan and Naproxen SodiumSumatriptan and Naproxen Sodium
65862-928Sumatriptan and Naproxen SodiumSumatriptan and Naproxen Sodium
71800-901Sumatriptan and Naproxen SodiumSumatriptan and Naproxen Sodium
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