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Data / Drug companies / Quality Care Products, LLC

Quality Care Products, LLC: 37 products in the FDA NDC directory, labeler code 55700

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

Quality Care Products, LLC (labeler code 55700) lists 37 products in the FDA National Drug Code Directory, covering 28 finished drugs by generic name. By type: 37 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on April 6, 2023.

The request: Watch Quality Care Products, LLC (FDA labeler code 55700): 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
55700
Products in commercial distribution
37
Packages
65
Finished drugs by generic name
28
Prescription products
37
Over the counter products
0
Controlled substance products
Schedule II 3, Schedule IV 6, Schedule V 4
Started marketing in the last 12 months
0
Products with a marketing end date set
37
Earliest marketing start
February 6, 2007
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)3594.6%
Authorized generics (NDA)25.4%

Products by type

TypeProductsShare
Prescription drugs37100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet1643.2%
Tablet, film coated821.6%
Capsule821.6%
Solution12.7%
Tablet, coated12.7%
Spray, metered12.7%
Patch12.7%
Tablet, extended release12.7%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Hydrocodone bitartrate and acetaminophen55700-992TabletGeneric drugs (ANDA)April 6, 2023
Tramadol Hydrochloride55700-997Tablet, coatedGeneric drugs (ANDA)February 7, 2023
Tramadol hydrochloride55700-996Tablet, extended releaseGeneric drugs (ANDA)January 24, 2023
Hydrocodone bitartrate and acetaminophen55700-991TabletGeneric drugs (ANDA)December 27, 2022
Pregabalin55700-964CapsuleGeneric drugs (ANDA)March 10, 2022
Gabapentin55700-950CapsuleGeneric drugs (ANDA)December 16, 2021
Gabapentin55700-949CapsuleGeneric drugs (ANDA)December 7, 2021
Naproxen55700-888TabletGeneric drugs (ANDA)February 26, 2021
Sumatriptan55700-899TabletGeneric drugs (ANDA)February 4, 2021
Fenofibrate55700-876TabletGeneric drugs (ANDA)July 21, 2020
Nabumetone55700-845TabletGeneric drugs (ANDA)February 28, 2020
Pregabalin55700-827CapsuleGeneric drugs (ANDA)December 3, 2019
Citalopram Hydrobromide55700-787TabletGeneric drugs (ANDA)August 30, 2019
Pregabalin55700-774CapsuleGeneric drugs (ANDA)July 19, 2019
Pregabalin55700-773CapsuleGeneric drugs (ANDA)July 19, 2019
Nabumetone55700-840TabletGeneric drugs (ANDA)June 26, 2019
Clindamycin hydrochloride55700-761CapsuleGeneric drugs (ANDA)June 7, 2019
Fluticasone Propionate55700-714Spray, meteredGeneric drugs (ANDA)January 4, 2019
Ondansetron Hydrochloride55700-631Tablet, film coatedGeneric drugs (ANDA)May 25, 2018
Ondansetron Hydrochloride55700-627Tablet, film coatedGeneric drugs (ANDA)May 18, 2018
Celecoxib55700-613CapsuleGeneric drugs (ANDA)May 4, 2018
Sulfamethoxazole and Trimethoprim55700-611TabletGeneric drugs (ANDA)May 4, 2018
Eszopiclone55700-610Tablet, film coatedGeneric drugs (ANDA)May 4, 2018
Diclofenac Sodium55700-591SolutionGeneric drugs (ANDA)March 9, 2018
Eszopiclone55700-581Tablet, film coatedGeneric drugs (ANDA)January 19, 2018

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.