NDC 0003-0894 – Eliquis
Apixaban 5 mg/1 · Tablet, Film Coated · Oral
Product NDC0003-0894
Product details
- Brand name
- Eliquis
- Generic name
- Apixaban
- Labeler
- E.R. Squibb & Sons, L.L.C.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- NDA · NDA202155
- Marketed since
- December 28, 2012
- Listing expires
- December 31, 2027
- Pharmacologic class
- Factor Xa Inhibitor
Active ingredients
- Apixaban 5 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 0003-0894-21 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0003-0894-21) | Dec 28, 2012 |
| 0003-0894-31 | 10 BLISTER PACK in 1 CARTON (0003-0894-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Dec 28, 2012 |
| 0003-0894-70 | 74 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0003-0894-70) | Jun 1, 2017 |
| 0003-0894-91 sample | 1 BLISTER PACK in 1 CARTON (0003-0894-91) / 14 TABLET, FILM COATED in 1 BLISTER PACK | Dec 28, 2012 |
Recalls mentioning this NDC
- D-0959-2017 Jul 19, 2017 · Class I
Labeling: Label Mix-up: One bottle of Eliquis 5 mg tablet was found to contain lower-strength Eliquis 2.5 mg tablets only instead of the labeled 5 mg tablets.
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