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Data / Drug companies / PuraCap Pharmaceutical LLC

PuraCap Pharmaceutical LLC: 21 products in the FDA NDC directory, labeler code 51013

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

PuraCap Pharmaceutical LLC (labeler code 51013) lists 21 products in the FDA National Drug Code Directory, covering 9 finished drugs by generic name. By type: 21 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on March 12, 2025.

The request: Watch PuraCap Pharmaceutical LLC (FDA labeler code 51013): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
51013
Products in commercial distribution
21
Packages
37
Finished drugs by generic name
9
Prescription products
0
Over the counter products
21
Flagged as original packager
21 of 21 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
June 9, 2016
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Over the counter monograph drugs1361.9%
Generic drugs (ANDA)838.1%

Products by type

TypeProductsShare
Over the counter drugs21100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Capsule, liquid filled1571.4%
Tablet, chewable314.3%
Tablet14.8%
Kit14.8%
Tablet, film coated14.8%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Ultra Concentrated Nighttime COLD AND FLU51013-668Capsule, liquid filledOver the counter monograph drugsMarch 12, 2025
Ultra Concentrated Daytime COLD AND FLU51013-667Capsule, liquid filledOver the counter monograph drugsMarch 12, 2025
Daytime COLD AND FLU51013-666Capsule, liquid filledOver the counter monograph drugsMarch 12, 2025
Stool Softener51013-819Capsule, liquid filledOver the counter monograph drugsNovember 30, 2024
Nighttime SLEEP AID51013-817Capsule, liquid filledOver the counter monograph drugsNovember 30, 2024
Naproxen sodium51013-137Capsule, liquid filledGeneric drugs (ANDA)March 20, 2018
Ibuprofen51013-429Capsule, liquid filledGeneric drugs (ANDA)February 13, 2018
Extra Strength Antacid51013-323Tablet, chewableOver the counter monograph drugsDecember 13, 2017
Motion Sickness Relief51013-322Tablet, chewableOver the counter monograph drugsNovember 28, 2017
Stomach Relief51013-321Tablet, chewableOver the counter monograph drugsNovember 28, 2017
Extra Strength Acetaminophen51013-320Tablet, film coatedOver the counter monograph drugsNovember 9, 2017
Ibuprofen51013-319TabletGeneric drugs (ANDA)November 9, 2017
Ibuprofen51013-422Capsule, liquid filledGeneric drugs (ANDA)November 1, 2017
Ibuprofen51013-421Capsule, liquid filledGeneric drugs (ANDA)August 29, 2017
Ibuprofen51013-410Capsule, liquid filledGeneric drugs (ANDA)July 14, 2017
Ibuprofen51013-405Capsule, liquid filledGeneric drugs (ANDA)July 14, 2017
Ibuprofen51013-103Capsule, liquid filledGeneric drugs (ANDA)October 12, 2016
Severe Sinus Congestion Allergy and Cough Formula51013-169Capsule, liquid filledOver the counter monograph drugsJune 29, 2016
DG Day Time Cold and Flu Formula and Night Time Cold and Flu Formula51013-168KitOver the counter monograph drugsJune 15, 2016
Daytime Severe Cold and Flu Relief51013-174Capsule, liquid filledOver the counter monograph drugsJune 13, 2016
Night Time Severe Cold and Flu Relief51013-175Capsule, liquid filledOver the counter monograph drugsJune 9, 2016

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.