Otezla

NDC 55513-516, apremilast, kit, from Amgen, Inc.

Product NDC: 55513-516
Status: Listed
Labeler: Amgen, Inc
Dosage form: KIT
Route: —
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: NDA
Application: NDA210745
DEA schedule: None

Request

curl https://api.healthcare.dev/v1/drugs/ndc/55513-516 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

None listed.

Package NDC	NDC-11	Package
55513-516-41	55513051641	1 BLISTER PACK in 1 CARTON (55513-516-41) / 1 KIT in 1 BLISTER PACK * 4 TABLET, FILM COATED in 1 BLISTER PACK (55513-523-04) * 19 TABLET, FILM COATED in 1 BLISTER PACK (55513-521-19) * 14 TABLET, FILM COATED in 1 BLISTER PACK (55513-522-14) * 4 TABLET, FILM COATED in 1 BLISTER PACK (55513-517-04)

Linked data

RxNorm, label and prices

RxNorm concepts

2724367{14 (24 HR apremilast 75 MG Extended Release Oral Tablet [Otezla]) / 4 (apremilast 10 MG Oral Tablet [Otezla]) / 4 (apremilast 20 MG Oral Tablet [Otezla]) / 19 (apremilast 30 MG Oral Tablet [Otezla]) } Pack [Otezla 28-Day 10/20/30/75 Starter Pack] (BPCK)

Related lookups

FDA label sections
GET /v1/drugs/labels/f6b1f516-4972-4d82-bced-113e47b41cc5

Use it

Look up 55513-516 from code or an agent

curl

curl https://api.healthcare.dev/v1/drugs/ndc/55513-516 \
  -H "Authorization: Bearer $HDEV_API_KEY"

MCP prompt

Using the healthcare.dev MCP server, look up NDC 55513-516. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.