NDC 72189-404

Imitrex

Sumatriptan

Imitrex is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Direct_rx. The primary component is Sumatriptan Succinate.

• Product ID: 72189-404_efb7ec4e-0a5e-2aae-e053-2a95a90aebf2
• NDC: 72189-404
• Product Type: Human Prescription Drug
• Proprietary Name: Imitrex
• Generic Name: Sumatriptan
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2022-12-13
• Marketing Category: ANDA /
• Application Number: ANDA078284
• Labeler Name: Direct_Rx
• Substance Name: SUMATRIPTAN SUCCINATE
• Active Ingredient Strength: 100 mg/1
• Pharm Classes: Serotonin 1b Receptor Agonists [MoA], Serotonin 1d Receptor Agonists [MoA], Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 72189-404-09

9 TABLET, FILM COATED in 1 BOTTLE (72189-404-09)

• Marketing Start Date: 2022-12-13
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

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

NDC	Brand Name	Generic Name
0173-0449	IMITREX	sumatriptan
0173-0478	IMITREX	sumatriptan
0173-0479	IMITREX	sumatriptan
0173-0523	IMITREX	sumatriptan
0173-0524	IMITREX	sumatriptan
0173-0735	IMITREX	sumatriptan
0173-0736	IMITREX	sumatriptan
0173-0737	IMITREX	sumatriptan
0173-0739	IMITREX	sumatriptan
21695-154	IMITREX	IMITREX
61919-950	IMITREX	IMITREX
0143-9638	SUMATRIPTAN	sumatriptan