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Data / Drug companies / Becton Dickinson and Company

Becton Dickinson and Company: 16 products in the FDA NDC directory, labeler code 17271

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

Becton Dickinson and Company (labeler code 17271) lists 16 products in the FDA National Drug Code Directory, covering 8 finished drugs by generic name. By type: 13 prescription drugs, 3 over the counter drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on November 14, 2025.

The request: Watch Becton Dickinson and Company (FDA labeler code 17271): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
17271
Products in commercial distribution
16
Packages
43
Finished drugs by generic name
8
Prescription products
13
Over the counter products
3
Flagged as original packager
16 of 16 products that carry the flag
Started marketing in the last 12 months
2
Earliest marketing start
March 1, 1989
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)1487.5%
Over the counter monograph drugs212.5%

Products by type

TypeProductsShare
Prescription drugs1381.2%
Over the counter drugs318.8%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Injection, solution1275%
Solution318.8%
Injection16.2%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Sterile Water17271-802InjectionGeneric drugs (ANDA)November 14, 2025
Sodium chloride17271-800Injection, solutionGeneric drugs (ANDA)November 14, 2025
Dextrose and Sodium Chloride17271-735Injection, solutionGeneric drugs (ANDA)October 26, 2020
Dextrose and Sodium Chloride17271-734Injection, solutionGeneric drugs (ANDA)October 26, 2020
Sterile Water17271-750Injection, solutionGeneric drugs (ANDA)February 28, 2020
3% Sodium Chloride17271-703Injection, solutionGeneric drugs (ANDA)February 28, 2020
Dextrose17271-721Injection, solutionGeneric drugs (ANDA)February 5, 2020
Lactated ringers17271-710Injection, solutionGeneric drugs (ANDA)January 28, 2019
Sodium chloride17271-700Injection, solutionGeneric drugs (ANDA)July 23, 2018
Sodium chloride17271-771Injection, solutionGeneric drugs (ANDA)September 19, 2017
Sodium chloride17271-701Injection, solutionGeneric drugs (ANDA)September 19, 2017
Dextrose17271-772Injection, solutionGeneric drugs (ANDA)October 21, 2016
Dextrose17271-720Injection, solutionGeneric drugs (ANDA)October 21, 2016
Bd e-z scrub17271-205SolutionOver the counter monograph drugsJune 1, 1995
BD E-Z Scrub 10717271-107SolutionGeneric drugs (ANDA)October 24, 1989
Bd e-z scrub17271-116SolutionOver the counter monograph drugsMarch 1, 1989

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.