NDC 55111-671 – Clopidogrel bisulfate
Clopidogrel Bisulfate 300 mg/1 · Tablet, Film Coated · Oral
Product NDC55111-671
Product details
- Brand name
- Clopidogrel bisulfate
- Generic name
- Clopidogrel bisulfate
- Labeler
- Dr.Reddy's Laboratories Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA091023
- Marketed since
- May 17, 2012
- Listing expires
- December 31, 2026
- Pharmacologic class
- P2Y12 Platelet Inhibitor
Active ingredients
- Clopidogrel Bisulfate 300 mg/1
Uses, dosage, side effects and warnings for Clopidogrel bisulfate →
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 55111-671-01 | 100 TABLET, FILM COATED in 1 BOTTLE (55111-671-01) | May 17, 2012 |
| 55111-671-05 | 500 TABLET, FILM COATED in 1 BOTTLE (55111-671-05) | May 17, 2012 |
| 55111-671-30 | 30 TABLET, FILM COATED in 1 BOTTLE (55111-671-30) | May 17, 2012 |
| 55111-671-31 | 5 BLISTER PACK in 1 CARTON (55111-671-31) / 6 TABLET, FILM COATED in 1 BLISTER PACK (55111-671-06) | May 17, 2012 |
| 55111-671-48 | 1 BLISTER PACK in 1 CARTON (55111-671-48) / 4 TABLET, FILM COATED in 1 BLISTER PACK | May 17, 2012 |
| 55111-671-78 | 10 BLISTER PACK in 1 CARTON (55111-671-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-671-79) | May 17, 2012 |
| 55111-671-81 | 3 BLISTER PACK in 1 CARTON (55111-671-81) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-671-79) | May 17, 2012 |
| 55111-671-90 | 90 TABLET, FILM COATED in 1 BOTTLE (55111-671-90) | May 17, 2012 |
Recalls mentioning this NDC
- D-0294-2019 Dec 19, 2018 · Class II
Failed dissolution specification -Two additional lots being recalled due to Out-of-Specification results observed for dissolution at 18th month stability testing. - D-0283-2019 Nov 28, 2018 · Class II
Failed Dissolution Specification: Out-of-Specification results were observed for dissolution at 18th month stability testing.
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