ELIQUIS
- Product NDC
- 0003-3765
- 11-digit product format
- 000033765
- Labeler code
- 0003
- Product ID
- 0003-3765_f96cb5ea-74e9-4751-883d-d18ef0d83640
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- apixaban
- Dosage form
- KIT
- Labeler
- E.R. Squibb & Sons, L.L.C.
- Application
- NDA202155
- Marketing category
- NDA
- Marketing start
- 2017-11-29
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ELIQUIS
- Brand name suffix
- 30-Day Starter Pack
- Listing expiration
- 2027-12-31