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Data / Drug companies / Contract Pharmacal Corp.

Contract Pharmacal Corp.: 26 products in the FDA NDC directory, labeler code 10267

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

Contract Pharmacal Corp. (labeler code 10267) lists 26 products in the FDA National Drug Code Directory, covering 4 finished drugs by generic name. By type: 15 drugs for further processing, 7 prescription drugs. Its main marketing category is drugs for further processing. The newest product started marketing on April 16, 2025.

The request: Watch Contract Pharmacal Corp. (FDA labeler code 10267): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
10267
Products in commercial distribution
26
Packages
50
Finished drugs by generic name
4
Prescription products
7
Over the counter products
4
Flagged as original packager
11 of 11 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
October 16, 2009
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Drugs for further processing1557.7%
Generic drugs (ANDA)1142.3%

Products by type

TypeProductsShare
Drugs for further processing1557.7%
Prescription drugs726.9%
Over the counter drugs415.4%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet, film coated1246.2%
Capsule623.1%
Tablet, chewable311.5%
Tablet311.5%
Tablet, coated27.7%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Cetirizine Hydrochloride 10 mg10267-3579Tablet, film coatedGeneric drugs (ANDA)April 16, 2025
Acetaminophen, caffeine10267-5808Tablet, film coatedDrugs for further processingOctober 10, 2024
Famotidine10267-5690Tablet, coatedGeneric drugs (ANDA)August 31, 2024
Famotidine10267-5689Tablet, coatedGeneric drugs (ANDA)August 31, 2024
Sennosides10267-0032Tablet, film coatedDrugs for further processingNovember 30, 2023
Acetaminophen10267-5923Tablet, film coatedDrugs for further processingSeptember 21, 2023
Doxepin Hydrochloride10267-5063CapsuleGeneric drugs (ANDA)January 24, 2021
Doxepin Hydrochloride10267-5062CapsuleGeneric drugs (ANDA)January 24, 2021
Doxepin Hydrochloride10267-5061CapsuleGeneric drugs (ANDA)January 24, 2021
Doxepin Hydrochloride10267-5060CapsuleGeneric drugs (ANDA)January 24, 2021
Doxepin Hydrochloride10267-5059CapsuleGeneric drugs (ANDA)January 24, 2021
Acetaminophen and pamabrom10267-5511Tablet, film coatedDrugs for further processingOctober 29, 2019
Magnesium salicylate, caffeine10267-5008Tablet, film coatedDrugs for further processingOctober 11, 2017
Acetaminophen, aspirin, caffeine10267-5005Tablet, film coatedDrugs for further processingMay 15, 2017
Caffeine10267-5010Tablet, film coatedDrugs for further processingMay 4, 2017
Sodium citrate10267-4243Tablet, chewableDrugs for further processingOctober 22, 2015
Calcium polycarbophil10267-0339Tablet, film coatedDrugs for further processingJune 22, 2015
Diphenhydramine hydrochloride10267-4690CapsuleDrugs for further processingMarch 11, 2015
Phenazopyridine hydrochloride10267-0317Tablet, film coatedDrugs for further processingSeptember 8, 2014
Ibuprofen10267-3909TabletGeneric drugs (ANDA)January 15, 2014
Ibuprofen10267-3852TabletGeneric drugs (ANDA)January 15, 2014
Ibuprofen10267-3846TabletGeneric drugs (ANDA)January 15, 2014
Pamabrom10267-0687Tablet, film coatedDrugs for further processingAugust 26, 2013
Dimenhydrinate10267-4186Tablet, chewableDrugs for further processingJuly 19, 2012
Dimenhydrinate10267-4215Tablet, chewableDrugs for further processingJanuary 20, 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.