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Data / Drug companies / Legacy Pharmaceutical Packaging, LLC

Legacy Pharmaceutical Packaging, LLC: 38 products in the FDA NDC directory, labeler code 68645

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

Legacy Pharmaceutical Packaging, LLC (labeler code 68645) lists 38 products in the FDA National Drug Code Directory, covering 17 finished drugs by generic name. By type: 38 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on March 10, 2022.

The request: Watch Legacy Pharmaceutical Packaging, LLC (FDA labeler code 68645): 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
68645
Products in commercial distribution
38
Packages
38
Finished drugs by generic name
17
Prescription products
38
Over the counter products
0
Started marketing in the last 12 months
0
Products with a marketing end date set
7
Earliest marketing start
January 12, 1973
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)38100%

Products by type

TypeProductsShare
Prescription drugs38100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet2668.4%
Tablet, film coated923.7%
Capsule25.3%
Tablet, extended release12.6%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Metformin68645-595Tablet, extended releaseGeneric drugs (ANDA)March 10, 2022
Famotidine68645-594Tablet, film coatedGeneric drugs (ANDA)September 22, 2021
Lisinopril68645-613TabletGeneric drugs (ANDA)August 17, 2021
Lisinopril68645-612TabletGeneric drugs (ANDA)August 17, 2021
Lisinopril68645-611TabletGeneric drugs (ANDA)August 17, 2021
Lisinopril68645-610TabletGeneric drugs (ANDA)August 17, 2021
Lisinopril68645-609TabletGeneric drugs (ANDA)August 17, 2021
Lisinopril68645-608TabletGeneric drugs (ANDA)August 17, 2021
Enalapril maleate68645-607TabletGeneric drugs (ANDA)October 1, 2020
Enalapril maleate68645-606TabletGeneric drugs (ANDA)October 1, 2020
Enalapril maleate68645-605TabletGeneric drugs (ANDA)April 28, 2020
Metformin hydrochloride68645-584TabletGeneric drugs (ANDA)June 7, 2019
Metformin hydrochloride68645-583TabletGeneric drugs (ANDA)June 7, 2019
Metformin hydrochloride68645-582TabletGeneric drugs (ANDA)June 7, 2019
Sertraline Hydrochloride68645-523TabletGeneric drugs (ANDA)July 21, 2016
Sertraline Hydrochloride68645-522TabletGeneric drugs (ANDA)July 21, 2016
Sertraline Hydrochloride68645-521TabletGeneric drugs (ANDA)July 21, 2016
Amlodipine Besylate68645-516TabletGeneric drugs (ANDA)July 1, 2016
Amlodipine Besylate68645-515TabletGeneric drugs (ANDA)July 1, 2016
Escitalopram Oxalate68645-520Tablet, film coatedGeneric drugs (ANDA)June 16, 2016
Escitalopram Oxalate68645-519Tablet, film coatedGeneric drugs (ANDA)June 16, 2016
Ibuprofen68645-563Tablet, film coatedGeneric drugs (ANDA)December 21, 2015
Ibuprofen68645-562Tablet, film coatedGeneric drugs (ANDA)December 21, 2015
Finasteride68645-541Tablet, film coatedGeneric drugs (ANDA)June 13, 2015
Clopidogrel68645-590Tablet, film coatedGeneric drugs (ANDA)May 17, 2012

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.