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Data / Drug companies / Pfizer Laboratories Div Pfizer Inc

Pfizer Laboratories Div Pfizer Inc: 19 products in the FDA NDC directory, labeler code 0013

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

Pfizer Laboratories Div Pfizer Inc (labeler code 0013) lists 19 products in the FDA National Drug Code Directory, covering 5 finished drugs by generic name. By type: 19 prescription drugs. Its main marketing category is biologics (BLA). The newest product started marketing on June 5, 2023.

The request: Watch Pfizer Laboratories Div Pfizer Inc (FDA labeler code 0013): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
0013
Products in commercial distribution
19
Packages
22
Finished drugs by generic name
5
Prescription products
19
Over the counter products
0
Flagged as original packager
17 of 17 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
June 20, 1950
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Biologics (BLA)1263.2%
New drug applications (NDA)736.8%

Products by type

TypeProductsShare
Prescription drugs19100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Kit1263.2%
Solution315.8%
System15.3%
Tablet, delayed release15.3%
Tablet15.3%
Injection, solution15.3%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Estring0013-1042SystemNew drug applications (NDA)June 5, 2023
Idamycin PFS0013-2596SolutionNew drug applications (NDA)February 17, 1997
Idamycin PFS0013-2586SolutionNew drug applications (NDA)February 17, 1997
Idamycin PFS0013-2576SolutionNew drug applications (NDA)February 17, 1997
Genotropin0013-2658KitBiologics (BLA)December 20, 1995
Genotropin0013-2657KitBiologics (BLA)December 20, 1995
Genotropin0013-2656KitBiologics (BLA)December 20, 1995
Genotropin0013-2655KitBiologics (BLA)December 20, 1995
Genotropin0013-2654KitBiologics (BLA)December 20, 1995
Genotropin0013-2653KitBiologics (BLA)December 20, 1995
Genotropin0013-2652KitBiologics (BLA)December 20, 1995
Genotropin0013-2651KitBiologics (BLA)December 20, 1995
Genotropin0013-2650KitBiologics (BLA)December 20, 1995
Genotropin0013-2649KitBiologics (BLA)December 20, 1995
Genotropin0013-2646KitBiologics (BLA)December 20, 1995
Genotropin0013-2626KitBiologics (BLA)December 20, 1995
Cyklokapron0013-1114Injection, solutionNew drug applications (NDA)December 30, 1986
Azulfidine EN-tabs0013-0102Tablet, delayed releaseNew drug applications (NDA)June 20, 1950
Azulfidine0013-0101TabletNew drug applications (NDA)June 20, 1950

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.