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Data / Drug companies / Quality Care Products, LLC

Quality Care Products, LLC: 20 products in the FDA NDC directory, labeler code 83008

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

Quality Care Products, LLC (labeler code 83008) lists 20 products in the FDA National Drug Code Directory, covering 16 finished drugs by generic name. By type: 20 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on September 18, 2024.

The request: Watch Quality Care Products, LLC (FDA labeler code 83008): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
83008
Products in commercial distribution
20
Packages
27
Finished drugs by generic name
16
Prescription products
20
Over the counter products
0
Controlled substance products
Schedule IV 1
Started marketing in the last 12 months
0
Products with a marketing end date set
20
Earliest marketing start
March 3, 2023
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)1995%
Authorized generics (NDA)15%

Products by type

TypeProductsShare
Prescription drugs20100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet735%
Tablet, film coated420%
Ointment210%
Tablet, delayed release15%
Tablet, film coated, extended release15%
System15%
Capsule15%
Solution15%
Gel15%
Tablet, extended release15%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Famotidine83008-091Tablet, film coatedGeneric drugs (ANDA)September 18, 2024
Losartan Potassium and Hydrochlorothiazide83008-086Tablet, film coatedGeneric drugs (ANDA)August 28, 2024
Irbesartan83008-085TabletGeneric drugs (ANDA)August 28, 2024
Irbesartan83008-084TabletGeneric drugs (ANDA)August 28, 2024
Bupropion Hydrochloride (XL)83008-082Tablet, film coated, extended releaseGeneric drugs (ANDA)August 28, 2024
Azithromycin Dihydrate83008-081Tablet, film coatedGeneric drugs (ANDA)August 28, 2024
Ondansetron Hydrochloride83008-074Tablet, film coatedGeneric drugs (ANDA)July 25, 2024
Lidocaine83008-067OintmentGeneric drugs (ANDA)July 23, 2024
Ibuprofen83008-066TabletGeneric drugs (ANDA)July 8, 2024
Lidocaine83008-044OintmentGeneric drugs (ANDA)June 26, 2024
Baclofen83008-062TabletGeneric drugs (ANDA)May 21, 2024
Atenolol83008-052TabletGeneric drugs (ANDA)January 25, 2024
Ibuprofen83008-050TabletGeneric drugs (ANDA)January 17, 2024
Diclofenac epolamine83008-036SystemAuthorized generics (NDA)August 15, 2023
Diclofenac Sodium83008-037GelGeneric drugs (ANDA)August 4, 2023
Amlodipine Besylate83008-035TabletGeneric drugs (ANDA)July 20, 2023
Pantoprazole Sodium83008-034Tablet, delayed releaseGeneric drugs (ANDA)July 18, 2023
Diclofenac sodium83008-019SolutionGeneric drugs (ANDA)May 2, 2023
Celecoxib83008-013CapsuleGeneric drugs (ANDA)April 25, 2023
Tramadol hydrochloride83008-009Tablet, extended releaseGeneric drugs (ANDA)March 3, 2023

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.