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Data / Drug companies / Allergan, Inc.

Allergan, Inc.: 8 products in the FDA NDC directory, labeler code 0430

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

Allergan, Inc. (labeler code 0430) lists 8 products in the FDA National Drug Code Directory, covering 2 finished drugs by generic name. By type: 5 prescription drugs, 3 drugs for further processing. Its main marketing category is new drug applications (NDA). The newest product started marketing on December 1, 2010.

The request: Watch Allergan, Inc. (FDA labeler code 0430): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
0430
Products in commercial distribution
8
Packages
10
Finished drugs by generic name
2
Prescription products
5
Over the counter products
0
Flagged as original packager
5 of 5 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
July 1, 2001
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)450%
Drugs for further processing337.5%
Generic drugs (ANDA)112.5%

Products by type

TypeProductsShare
Prescription drugs562.5%
Drugs for further processing337.5%

Drugs it lists

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

DrugProductsCompanies listing it
Risedronate sodium39
Estradiol153

Dosage forms

Dosage formProductsShare
Tablet, film coated450%
Tablet, delayed release225%
Kit112.5%
Cream112.5%

Pharmacologic classes

FDA established pharmacologic classes of its products.

ClassProducts
Bisphosphonate3
Estrogen1

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Atelvia0430-0979Tablet, delayed releaseNew drug applications (NDA)December 1, 2010
Risedronate sodium0430-0970Tablet, delayed releaseDrugs for further processingDecember 1, 2010
Lo Loestrin Fe0430-0420KitNew drug applications (NDA)December 1, 2010
Risedronate sodium0430-0487Tablet, film coatedDrugs for further processingApril 22, 2008
Actonel0430-0478Tablet, film coatedNew drug applications (NDA)April 22, 2008
Risedronate sodium0430-0473Tablet, film coatedDrugs for further processingMay 17, 2002
Actonel0430-0472Tablet, film coatedNew drug applications (NDA)May 17, 2002
Estrace0430-3754CreamGeneric drugs (ANDA)July 1, 2001

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.