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Data / Drug companies / Aaa Pharmaceutical, Inc.

Aaa Pharmaceutical, Inc.: 28 products in the FDA NDC directory, labeler code 57344

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

Aaa Pharmaceutical, Inc. (labeler code 57344) lists 28 products in the FDA National Drug Code Directory, covering 13 finished drugs by generic name. By type: 28 over the counter drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on April 30, 2026.

The request: Watch Aaa Pharmaceutical, Inc. (FDA labeler code 57344): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
57344
Products in commercial distribution
28
Packages
51
Finished drugs by generic name
13
Prescription products
0
Over the counter products
28
Flagged as original packager
23 of 23 products that carry the flag
Started marketing in the last 12 months
2
Earliest marketing start
April 1, 2012
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)1450%
Over the counter monograph drugs1450%

Products by type

TypeProductsShare
Over the counter drugs28100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet, coated1760.7%
Tablet621.4%
Tablet, extended release310.7%
Tablet, delayed release27.1%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Naproxen Sodium57344-244Tablet, coatedGeneric drugs (ANDA)April 30, 2026
Ibuprofen57344-212Tablet, coatedGeneric drugs (ANDA)February 16, 2026
Arthritis Pain57344-200Tablet, extended releaseGeneric drugs (ANDA)September 12, 2025
Pain Relief57344-103TabletOver the counter monograph drugsJune 2, 2025
Ibuprofen57344-309Tablet, coatedGeneric drugs (ANDA)December 5, 2024
8HR Muscle Aches and Pain57344-201Tablet, extended releaseGeneric drugs (ANDA)April 15, 2024
Stay Awake57344-220TabletOver the counter monograph drugsApril 1, 2024
Mucus Relief57344-203Tablet, extended releaseGeneric drugs (ANDA)February 1, 2024
Migraine Relief57344-205TabletGeneric drugs (ANDA)May 3, 2023
Allergy Relief57344-292TabletGeneric drugs (ANDA)July 6, 2021
Allergy Relief57344-193TabletGeneric drugs (ANDA)August 14, 2020
Allergy Multi Symptom57344-928Tablet, coatedOver the counter monograph drugsAugust 1, 2020
Sinus and Headache57344-923Tablet, coatedOver the counter monograph drugsAugust 1, 2020
Ibuprofen57344-811Tablet, coatedGeneric drugs (ANDA)February 1, 2020
Diphenhydramine Hydrochloride57344-091Tablet, coatedOver the counter monograph drugsOctober 5, 2018
Allergy Relief57344-194Tablet, coatedGeneric drugs (ANDA)October 1, 2018
Aspirin57344-146Tablet, delayed releaseOver the counter monograph drugsSeptember 1, 2017
Aspirin57344-018Tablet, coatedOver the counter monograph drugsSeptember 1, 2017
Aspirin57344-080Tablet, delayed releaseOver the counter monograph drugsJuly 1, 2017
Pain Relief57344-170Tablet, coatedOver the counter monograph drugsJanuary 1, 2015
Ibuprofen57344-110Tablet, coatedGeneric drugs (ANDA)September 1, 2014
Pain Relief57344-301TabletOver the counter monograph drugsDecember 13, 2012
Ibuprofen57344-109Tablet, coatedGeneric drugs (ANDA)October 1, 2012
Acetaminophen PM57344-095Tablet, coatedOver the counter monograph drugsOctober 1, 2012
Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride57344-163Tablet, coatedOver the counter monograph drugsAugust 2, 2012

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.