NDC 62756-522 – Sumatriptan succinate
Sumatriptan Succinate 100 mg/1 · Tablet, Film Coated · Oral
Product NDC62756-522
Product details
- Brand name
- Sumatriptan succinate
- Generic name
- Sumatriptan succinate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078295
- Marketed since
- August 10, 2009
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin-1b and Serotonin-1d Receptor Agonist
Active ingredients
- Sumatriptan Succinate 100 mg/1
Uses, dosage, side effects and warnings for Sumatriptan Succinate →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 62756-522-01 | 3 BLISTER PACK in 1 CARTON (62756-522-01) / 9 TABLET, FILM COATED in 1 BLISTER PACK | Nov 1, 2020 |
| 62756-522-08 | 100 TABLET, FILM COATED in 1 BOTTLE (62756-522-08) | Aug 10, 2009 |
| 62756-522-18 | 1000 TABLET, FILM COATED in 1 BOTTLE (62756-522-18) | Aug 10, 2009 |
| 62756-522-83 | 30 TABLET, FILM COATED in 1 BOTTLE (62756-522-83) | Aug 10, 2009 |
| 62756-522-93 | 9 BLISTER PACK in 1 CARTON (62756-522-93) / 1 TABLET, FILM COATED in 1 BLISTER PACK | Aug 10, 2009 |
Recalls mentioning this NDC
- D-1111-2022 Jun 15, 2022 · Class II
cGMP deviations: Temperature abuse - D-0659-2020 Jan 22, 2020 · Class II
Failed Impurities/Degradation Specifications; out-of-specification results obtained for related substance.
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