NDC 0173-0739 – Imitrex
Sumatriptan Succinate 4 mg/.5mL · Injection · Subcutaneous
Product NDC0173-0739
Product details
- Brand name
- Imitrex
- Generic name
- Sumatriptan
- Labeler
- GlaxoSmithKline LLC
- Dosage form
- Injection
- Route
- Subcutaneous
- Marketing category
- NDA · NDA020080
- Marketed since
- April 6, 2006
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin-1b and Serotonin-1d Receptor Agonist
Active ingredients
- Sumatriptan Succinate 4 mg/.5mL
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0173-0739-00 | 2 SYRINGE in 1 PACKAGE (0173-0739-00) / .5 mL in 1 SYRINGE | Apr 6, 2006 |
| 0173-0739-02 | 2 SYRINGE in 1 CARTON (0173-0739-02) / .5 mL in 1 SYRINGE | Apr 6, 2006 |
Recalls mentioning this NDC
- D-387-2014 Jan 1, 2014 · Class II
Lack of Assurance of Sterility: A small number of pre-filled syringes may contain needles which protrude through the needle shield.
Other Imitrex products
- 0173-0478 Sumatriptan Succinate 6 mg/.5mL · Injection · GlaxoSmithKline LLC
- 0173-0479 Sumatriptan Succinate 6 mg/.5mL · Injection · GlaxoSmithKline LLC
- 0173-0735 Sumatriptan Succinate 25 mg/1 · Tablet, Film Coated · GlaxoSmithKline LLC
- 0173-0736 Sumatriptan Succinate 50 mg/1 · Tablet, Film Coated · GlaxoSmithKline LLC
- 0173-0737 Sumatriptan Succinate 100 mg/1 · Tablet, Film Coated · GlaxoSmithKline LLC