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Data / Drug companies / AbbVie Inc.

AbbVie Inc.: 10 products in the FDA NDC directory, labeler code 0032

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

AbbVie Inc. (labeler code 0032) lists 10 products in the FDA National Drug Code Directory, covering 1 finished drug by generic name. By type: 10 prescription drugs. Its main marketing category is biologics (BLA). The newest product started marketing on October 12, 2023.

The request: Watch AbbVie Inc. (FDA labeler code 0032): each new product listing and each discontinued product. $10 of work on sign-up, no card.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
0032
Products in commercial distribution
10
Packages
26
Finished drugs by generic name
1
Prescription products
10
Over the counter products
0
Flagged as original packager
10 of 10 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
April 30, 2009
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Biologics (BLA)10100%

Products by type

TypeProductsShare
Prescription drugs10100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

DrugProductsCompanies listing it
Pancrelipase103

Dosage forms

Dosage formProductsShare
Capsule, delayed release pellets880%
Capsule, delayed release220%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Creon0032-2637Capsule, delayed release pelletsBiologics (BLA)October 12, 2023
Creon0032-2636Capsule, delayed release pelletsBiologics (BLA)October 12, 2023
Creon0032-0047Capsule, delayed release pelletsBiologics (BLA)October 12, 2023
Creon0032-0046Capsule, delayed release pelletsBiologics (BLA)October 12, 2023
Creon0032-0045Capsule, delayed releaseBiologics (BLA)October 12, 2023
Creon0032-3016Capsule, delayed release pelletsBiologics (BLA)March 14, 2013
Creon0032-1224Capsule, delayed release pelletsBiologics (BLA)April 30, 2009
Creon0032-1212Capsule, delayed release pelletsBiologics (BLA)April 30, 2009
Creon0032-1206Capsule, delayed release pelletsBiologics (BLA)April 30, 2009
Creon0032-1203Capsule, delayed releaseBiologics (BLA)April 30, 2009

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.