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ELIQUIS
ELIQUIS - 0003-0894-31 - (apixaban)
Drug Information of ELIQUIS
| Product NDC: | 0003-0894 |
| Proprietary Name: | ELIQUIS |
| Non Proprietary Name: | apixaban |
| Active Ingredient(s): | 5 mg/1 & nbsp; apixaban |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ELIQUIS
| Product NDC: | 0003-0894 |
| Labeler Name: | E.R. Squibb & Sons, L.L.C. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA202155 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20121228 |
Package Information of ELIQUIS
| Package NDC: | 0003-0894-31 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (0003-0894-31) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of ELIQUIS
| NDC Code | 0003-0894-31 |
| Proprietary Name | ELIQUIS |
| Package Description | 10 BLISTER PACK in 1 CARTON (0003-0894-31) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 0003-0894 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | apixaban |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20121228 |
| Marketing Category Name | NDA |
| Labeler Name | E.R. Squibb & Sons, L.L.C. |
| Substance Name | APIXABAN |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
