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Data / Drug companies / Quality Care Products LLC

Quality Care Products LLC: 7 products in the FDA NDC directory, labeler code 49999

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

Quality Care Products LLC (labeler code 49999) lists 7 products in the FDA National Drug Code Directory, covering 7 finished drugs by generic name. By type: 7 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on April 16, 2012.

The request: Watch Quality Care Products LLC (FDA labeler code 49999): 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
49999
Products in commercial distribution
7
Packages
19
Finished drugs by generic name
7
Prescription products
7
Over the counter products
0
Controlled substance products
Schedule II 2
Started marketing in the last 12 months
0
Products with a marketing end date set
7
Earliest marketing start
June 10, 2010
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)7100%

Products by type

TypeProductsShare
Prescription drugs7100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet457.1%
Tablet, extended release114.3%
Capsule114.3%
Capsule, delayed release114.3%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Doxycycline Hyclate49999-126CapsuleGeneric drugs (ANDA)April 16, 2012
Oxycodone Hydchloride49999-899TabletGeneric drugs (ANDA)December 20, 2011
Orphenadrine Citrate49999-046Tablet, extended releaseGeneric drugs (ANDA)February 7, 2011
Tizanidine Hydrochloride49999-347TabletGeneric drugs (ANDA)November 23, 2010
Omeprazole49999-265Capsule, delayed releaseGeneric drugs (ANDA)October 13, 2010
Meloxicam49999-869TabletGeneric drugs (ANDA)September 17, 2010
Oxycodone and Acetaminophen49999-852TabletGeneric drugs (ANDA)June 10, 2010

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.