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Data / Drug companies / Aurohealth LLC

Aurohealth LLC: 179 products in the FDA NDC directory, labeler code 58602

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

Aurohealth LLC (labeler code 58602) lists 179 products in the FDA National Drug Code Directory, covering 44 finished drugs by generic name. By type: 179 over the counter drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on September 28, 2026.

The request: Watch Aurohealth LLC (FDA labeler code 58602): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
58602
Products in commercial distribution
179
Packages
786
Finished drugs by generic name
44
Prescription products
0
Over the counter products
179
Flagged as original packager
167 of 167 products that carry the flag
Started marketing in the last 12 months
26
Earliest marketing start
February 2, 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)15486%
Over the counter monograph drugs2514%

Products by type

TypeProductsShare
Over the counter drugs179100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet3821.2%
Tablet, extended release2111.7%
Tablet, film coated1910.6%
Suspension158.4%
Capsule126.7%
Solution116.1%
Lozenge105.6%
Tablet, orally disintegrating84.5%
Capsule, liquid filled73.9%
Spray, metered63.4%
Capsule, delayed release63.4%
Aerosol, foam42.2%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Ibuprofen58602-913TabletGeneric drugs (ANDA)September 28, 2026
Polyethylene Glycol 335058602-910Powder, for solutionGeneric drugs (ANDA)September 28, 2026
Minoxidil 5% (for men)58602-614Aerosol, foamGeneric drugs (ANDA)September 25, 2026
Omeprazole and sodium bicarbonate58602-732CapsuleGeneric drugs (ANDA)September 22, 2026
Fexofenadine hydrochloride58602-427SuspensionGeneric drugs (ANDA)August 31, 2026
Childrens triamcinolone acetonide58602-037Spray, meteredGeneric drugs (ANDA)August 11, 2026
Triamcinolone acetonide58602-035Spray, meteredGeneric drugs (ANDA)August 11, 2026
Childrens Pain and Fever58602-171SuspensionOver the counter monograph drugsJuly 30, 2026
Childrens Pain and Fever58602-164SuspensionOver the counter monograph drugsJuly 30, 2026
Childrens Pain and Fever58602-167SuspensionOver the counter monograph drugsJuly 27, 2026
Childrens Pain and Fever58602-166SuspensionOver the counter monograph drugsJuly 23, 2026
Childrens Pain and Fever58602-165SuspensionOver the counter monograph drugsJuly 23, 2026
Guaifenesin58602-857Tablet, extended releaseGeneric drugs (ANDA)July 3, 2026
Minoxidil 5% (for women)58602-104Aerosol, foamGeneric drugs (ANDA)June 19, 2026
Acetaminophen Regular Strength58602-748TabletOver the counter monograph drugsJune 8, 2026
Infants Pain and Fever58602-173SuspensionOver the counter monograph drugsMay 18, 2026
INFANTS Pain and Fever58602-172SuspensionOver the counter monograph drugsMay 18, 2026
Dextromethorphan polistirex58602-618Suspension, extended releaseGeneric drugs (ANDA)April 17, 2026
Dextromethorphan polistirex58602-617Suspension, extended releaseGeneric drugs (ANDA)April 17, 2026
Dextromethorphan polistirex58602-611Suspension, extended releaseGeneric drugs (ANDA)April 15, 2026
Dextromethorphan polistirex58602-610Suspension, extended releaseGeneric drugs (ANDA)April 15, 2026
Infants Pain and Fever58602-169SuspensionOver the counter monograph drugsMarch 20, 2026
INFANTS Pain and Fever58602-168SuspensionOver the counter monograph drugsMarch 20, 2026
Pseudoephedrine Hydrochloride58602-884Tablet, extended releaseGeneric drugs (ANDA)December 29, 2025
Loperamide hydrochloride58602-727Capsule, liquid filledGeneric drugs (ANDA)December 29, 2025

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.