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Data / Drug companies / Aphena Pharma Solutions - Tennessee, LLC

Aphena Pharma Solutions - Tennessee, LLC: 69 products in the FDA NDC directory, labeler code 43353

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

Aphena Pharma Solutions - Tennessee, LLC (labeler code 43353) lists 69 products in the FDA National Drug Code Directory, covering 42 finished drugs by generic name. By type: 67 prescription drugs, 2 over the counter drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on June 20, 2017.

The request: Watch Aphena Pharma Solutions - Tennessee, LLC (FDA labeler code 43353): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
43353
Products in commercial distribution
69
Packages
252
Finished drugs by generic name
42
Prescription products
67
Over the counter products
2
Controlled substance products
Schedule IV 5, Schedule V 2
Started marketing in the last 12 months
0
Earliest marketing start
January 12, 1973
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)6289.9%
Authorized generics (NDA)34.3%
New drug applications (NDA)34.3%
Over the counter monograph drugs11.4%

Products by type

TypeProductsShare
Prescription drugs6797.1%
Over the counter drugs22.9%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet4666.7%
Capsule811.6%
Tablet, film coated68.7%
Tablet, extended release57.2%
Capsule, liquid filled22.9%
Tablet, delayed release11.4%
Capsule, delayed release11.4%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Diphenoxylate Hydrochloride and Atropine Sulfate43353-594TabletGeneric drugs (ANDA)June 20, 2017
Valproic Acid43353-279Capsule, liquid filledGeneric drugs (ANDA)July 15, 2016
Naproxen43353-218TabletGeneric drugs (ANDA)June 10, 2016
Naproxen43353-216TabletGeneric drugs (ANDA)June 10, 2016
Naproxen43353-211TabletGeneric drugs (ANDA)June 10, 2016
HydrALAZINE Hydrochloride43353-205TabletGeneric drugs (ANDA)May 20, 2016
Oxybutynin Chloride Extended Release43353-322Tablet, extended releaseGeneric drugs (ANDA)March 9, 2016
Oxybutynin Chloride Extended Release43353-284Tablet, extended releaseGeneric drugs (ANDA)March 9, 2016
Oxybutynin Chloride Extended Release43353-282Tablet, extended releaseGeneric drugs (ANDA)March 9, 2016
Tacrolimus43353-317CapsuleGeneric drugs (ANDA)November 18, 2015
Ergocalciferol43353-238Capsule, liquid filledGeneric drugs (ANDA)July 23, 2015
Sodium bicarbonate43353-162TabletOver the counter monograph drugsMay 1, 2015
Warfarin Sodium43353-054TabletGeneric drugs (ANDA)April 8, 2015
Warfarin Sodium43353-053TabletGeneric drugs (ANDA)April 8, 2015
Warfarin Sodium43353-033TabletGeneric drugs (ANDA)April 8, 2015
Warfarin Sodium43353-029TabletGeneric drugs (ANDA)April 8, 2015
Warfarin Sodium43353-023TabletGeneric drugs (ANDA)April 8, 2015
Warfarin Sodium43353-021TabletGeneric drugs (ANDA)April 8, 2015
Gabapentin43353-081CapsuleGeneric drugs (ANDA)March 17, 2014
Lisinopril43353-301TabletGeneric drugs (ANDA)March 15, 2014
Lisinopril43353-298TabletGeneric drugs (ANDA)March 15, 2014
Lisinopril43353-271TabletGeneric drugs (ANDA)March 15, 2014
Lisinopril43353-270TabletGeneric drugs (ANDA)March 15, 2014
Lisinopril43353-009TabletGeneric drugs (ANDA)March 15, 2014
Carbamazepine43353-953TabletGeneric drugs (ANDA)March 7, 2014

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.