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Data / Drug companies / Allergan, Inc.

Allergan, Inc.: 76 products in the FDA NDC directory, labeler code 0456

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

Allergan, Inc. (labeler code 0456) lists 76 products in the FDA National Drug Code Directory, covering 12 finished drugs by generic name. By type: 45 prescription drugs, 31 drugs for further processing. Its main marketing category is new drug applications (NDA). The newest product started marketing on March 24, 2023.

The request: Watch Allergan, Inc. (FDA labeler code 0456): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
0456
Products in commercial distribution
76
Packages
99
Finished drugs by generic name
12
Prescription products
45
Over the counter products
0
Flagged as original packager
34 of 34 products that carry the flag
Started marketing in the last 12 months
0
Products with a marketing end date set
2
Earliest marketing start
April 1, 1996
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
New drug applications (NDA)3748.7%
Drugs for further processing3140.8%
Other unapproved drugs810.5%

Products by type

TypeProductsShare
Prescription drugs4559.2%
Drugs for further processing3140.8%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet2836.8%
Tablet, film coated2026.3%
Capsule, extended release810.5%
Capsule810.5%
Capsule, gelatin coated67.9%
Powder, for solution33.9%
Kit33.9%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Fetzima0456-2200KitNew drug applications (NDA)March 24, 2023
Linaclotide0456-1206Capsule, gelatin coatedDrugs for further processingJanuary 30, 2017
Linzess0456-1203Capsule, gelatin coatedNew drug applications (NDA)January 30, 2017
Memantine hydrochloride and donepezil hydrochloride0456-1222CapsuleDrugs for further processingJuly 18, 2016
Namzaric0456-1221CapsuleNew drug applications (NDA)July 18, 2016
Memantine hydrochloride and donepezil hydrochloride0456-1208CapsuleDrugs for further processingJuly 18, 2016
Namzaric0456-1207CapsuleNew drug applications (NDA)July 18, 2016
Asenapine maleate0456-2404TabletDrugs for further processingDecember 30, 2014
Saphris0456-2402TabletNew drug applications (NDA)December 30, 2014
Avycaz0456-2700Powder, for solutionNew drug applications (NDA)December 26, 2014
Memantine hydrochloride and donepezil hydrochloride0456-1238CapsuleDrugs for further processingDecember 24, 2014
Namzaric0456-1228CapsuleNew drug applications (NDA)December 24, 2014
Memantine hydrochloride and donepezil hydrochloride0456-1215CapsuleDrugs for further processingDecember 24, 2014
Namzaric0456-1214CapsuleNew drug applications (NDA)December 24, 2014
Asenapine maleate0456-2412TabletDrugs for further processingSeptember 30, 2013
Saphris0456-2410TabletNew drug applications (NDA)September 30, 2013
Asenapine maleate0456-2407TabletDrugs for further processingSeptember 30, 2013
Saphris0456-2405TabletNew drug applications (NDA)September 30, 2013
Fetzima0456-2280Capsule, extended releaseNew drug applications (NDA)July 25, 2013
Fetzima0456-2240Capsule, extended releaseNew drug applications (NDA)July 25, 2013
Fetzima0456-2220Capsule, extended releaseNew drug applications (NDA)July 25, 2013
Fetzima0456-2212Capsule, extended releaseNew drug applications (NDA)July 25, 2013
Fetzima0456-2202KitNew drug applications (NDA)July 25, 2013
Linaclotide0456-1205Capsule, gelatin coatedDrugs for further processingSeptember 8, 2012
Linaclotide0456-1204Capsule, gelatin coatedDrugs for further processingSeptember 8, 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.