ELIQUIS
- Product NDC
- 0003-3764
- 11-digit product format
- 000033764
- Labeler code
- 0003
- Product ID
- 0003-3764_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
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0003-3764-74 | ELIQUIS30-Day Starter Pack | 1 in 1 CARTON | KIT | 1 | | 30 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| apixaban | ACTIVE INGREDIENT | 3Z9Y7UWC1J | ELIQUIS (APIXABAN) TABLET, FILM COATED [E.R. SQUIBB & SONS, L.L.C.] | 7 | |
| apixaban | ACTIVE MOIETY | 3Z9Y7UWC1J | ELIQUIS (APIXABAN) TABLET, FILM COATED [E.R. SQUIBB & SONS, L.L.C.] | 7 | |
| anhydrous lactose | INACTIVE INGREDIENT | 3SY5LH9PMK | ELIQUIS (APIXABAN) TABLET, FILM COATED [E.R. SQUIBB & SONS, L.L.C.] | 7 | |
| cellulose, microcrystalline | INACTIVE INGREDIENT | OP1R32D61U | ELIQUIS (APIXABAN) TABLET, FILM COATED [E.R. SQUIBB & SONS, L.L.C.] | 7 | |
| croscarmellose sodium | INACTIVE INGREDIENT | M28OL1HH48 | ELIQUIS (APIXABAN) TABLET, FILM COATED [E.R. SQUIBB & SONS, L.L.C.] | 7 | |
| ferric oxide red | INACTIVE INGREDIENT | 1K09F3G675 | ELIQUIS (APIXABAN) TABLET, FILM COATED [E.R. SQUIBB & SONS, L.L.C.] | 7 | |
| ferric oxide yellow | INACTIVE INGREDIENT | EX438O2MRT | ELIQUIS (APIXABAN) TABLET, FILM COATED [E.R. SQUIBB & SONS, L.L.C.] | 7 | |
| hypromelloses | INACTIVE INGREDIENT | 3NXW29V3WO | ELIQUIS (APIXABAN) TABLET, FILM COATED [E.R. SQUIBB & SONS, L.L.C.] | 7 | |
| lactose monohydrate | INACTIVE INGREDIENT | EWQ57Q8I5X | ELIQUIS (APIXABAN) TABLET, FILM COATED [E.R. SQUIBB & SONS, L.L.C.] | 7 | |
| magnesium stearate | INACTIVE INGREDIENT | 70097M6I30 | ELIQUIS (APIXABAN) TABLET, FILM COATED [E.R. SQUIBB & SONS, L.L.C.] | 7 | |
| sodium lauryl sulfate | INACTIVE INGREDIENT | 368GB5141J | ELIQUIS (APIXABAN) TABLET, FILM COATED [E.R. SQUIBB & SONS, L.L.C.] | 7 | |
| titanium dioxide | INACTIVE INGREDIENT | 15FIX9V2JP | ELIQUIS (APIXABAN) TABLET, FILM COATED [E.R. SQUIBB & SONS, L.L.C.] | 7 | |
| triacetin | INACTIVE INGREDIENT | XHX3C3X673 | ELIQUIS (APIXABAN) TABLET, FILM COATED [E.R. SQUIBB & SONS, L.L.C.] | 7 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0003-3764 | ELIQUIS (APIXABAN) TABLET, FILM COATED ELIQUIS 30-DAY STARTER PACK (APIXABAN) KIT [E.R. SQUIBB & SONS, L.L.C.] | 30 | Current NDC, Legacy NDC, 1 package rows | 20250504_e9481622-7cc6-418a-acb6-c5450daae9b0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0003-3764-74 | 00003376474 | 1 KIT in 1 CARTON (0003-3764-74) * 32 TABLET, COATED in 1 BLISTER PACK * 42 TABLET, COATED in 1 BLISTER PACK | 1 kit | 2017-11-30 | 0000-00-00 | No | No | Current |