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Data / Drug companies / Acella Pharmaceuticals, LLC

Acella Pharmaceuticals, LLC: 40 products in the FDA NDC directory, labeler code 42192

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

Acella Pharmaceuticals, LLC (labeler code 42192) lists 40 products in the FDA National Drug Code Directory, covering 17 finished drugs by generic name. By type: 40 prescription drugs. Its main marketing category is other unapproved drugs. The newest product started marketing on October 31, 2026.

The request: Watch Acella Pharmaceuticals, LLC (FDA labeler code 42192): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
42192
Products in commercial distribution
40
Packages
65
Finished drugs by generic name
17
Prescription products
40
Over the counter products
0
Flagged as original packager
28 of 28 products that carry the flag
Started marketing in the last 12 months
2
Products with a marketing end date set
3
Earliest marketing start
October 1, 1990
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Other unapproved drugs3075%
Generic drugs (ANDA)717.5%
New drug applications (NDA)25%
Authorized generics (NDA)12.5%

Products by type

TypeProductsShare
Prescription drugs40100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet922.5%
Solution615%
Liquid512.5%
Cream410%
Capsule, gelatin coated37.5%
Syrup25%
Rinse25%
Kit25%
Gel12.5%
Suspension12.5%
Tablet, coated12.5%
Capsule, coated12.5%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
NP Thyroid 18042192-376TabletOther unapproved drugsOctober 31, 2026
Baclofen42192-631SolutionNew drug applications (NDA)October 26, 2026
Brompheniramine Maleate, Pseudoephedrine Hydrochloride, Dextromethorphan Hydrobromide42192-630SyrupGeneric drugs (ANDA)February 1, 2025
Pyridostigmine Bromide42192-626SolutionGeneric drugs (ANDA)October 9, 2023
Levonorgestrel and ethinyl estradiol42192-623KitNew drug applications (NDA)August 21, 2023
Phenytoin sodium42192-614InjectionGeneric drugs (ANDA)December 1, 2021
Nicotinamide42192-374TabletOther unapproved drugsMay 25, 2021
Naproxen42192-619SuspensionAuthorized generics (NDA)November 12, 2020
Doxycycline42192-501Tablet, coatedGeneric drugs (ANDA)August 21, 2020
Ciclopirox42192-715SolutionGeneric drugs (ANDA)November 4, 2019
NP Thyroid 12042192-328TabletOther unapproved drugsJune 12, 2017
Sodium Sulfacetamide 9.8% and Sulfur 4.8% Cleanser42192-156LiquidOther unapproved drugsDecember 12, 2016
NP Thyroid 1542192-327TabletOther unapproved drugsNovember 16, 2016
Brompheniramine Maleate, Pseudoephedrine Hydrochloride, Dextromethorphan Hydrobromide42192-607SyrupGeneric drugs (ANDA)September 21, 2016
Hydroquinone 4%42192-151CreamOther unapproved drugsSeptember 10, 2014
Sodium Sulfacetamide 10 Sulfur 2 cream42192-150CreamOther unapproved drugsAugust 21, 2014
Sodium sulfacetamide, sulfur42192-149CreamOther unapproved drugsAugust 14, 2014
Sodium Sulfacetamide 10 Sulfur 2 Cleanser42192-147SolutionOther unapproved drugsAugust 14, 2014
Sodium sulfacetamide, sulfur42192-139CreamOther unapproved drugsJune 11, 2014
Sodium Sulfacetamide 9 Sulfur 4.5 Wash42192-144RinseOther unapproved drugsMarch 20, 2013
Gabapentin42192-608SolutionGeneric drugs (ANDA)October 1, 2012
Sodium Sulfacetamide 10 Sulfur 5 Cleanser42192-136RinseOther unapproved drugsApril 20, 2012
Ciclopirox42192-714KitOther unapproved drugsOctober 10, 2011
Salicylic acid42192-135LiquidOther unapproved drugsOctober 10, 2011
Hyoscyamine Sulfate TAB42192-340TabletOther unapproved drugsMay 19, 2011

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.