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Data / Drug companies / Cambrex Karlskoga AB

Cambrex Karlskoga AB: 13 products in the FDA NDC directory, labeler code 12651

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

Cambrex Karlskoga AB (labeler code 12651) lists 13 products in the FDA National Drug Code Directory. By type: 13 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on August 5, 2026.

The request: Watch Cambrex Karlskoga AB (FDA labeler code 12651): each new product listing and each discontinued product. $10 of work on sign-up, no card.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
12651
Products in commercial distribution
13
Packages
29
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Started marketing in the last 12 months
1
Earliest marketing start
March 21, 1988
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients13100%

Products by type

TypeProductsShare
Bulk ingredients13100%

Dosage forms

Dosage formProductsShare
Powder13100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Zongertinib12651-126PowderBulk ingredientsAugust 5, 2026
Olanzapine12651-125PowderBulk ingredientsOctober 31, 2023
Lidocaine12651-124PowderBulk ingredientsOctober 12, 2023
Momelotinib dihydrochloride monohydrate12651-123PowderBulk ingredientsFebruary 8, 2023
Tesofensine/ns2330 citrate12651-121PowderBulk ingredientsJanuary 19, 2021
Berotralstat dihydrochloride12651-120PowderBulk ingredientsJanuary 13, 2021
4-amiinobenzoic acid12651-119PowderBulk ingredientsMarch 5, 2020
Rivastigmine12651-118PowderBulk ingredientsFebruary 22, 2017
Bupivacaine hydrochloride12651-111PowderBulk ingredientsJuly 19, 2016
Bupivacaine base12651-116PowderBulk ingredientsAugust 1, 2011
Lidocaine hydrochloride12651-113PowderBulk ingredientsJune 30, 2006
Benzoyl peroxide, hydrous12651-115PowderBulk ingredientsDecember 27, 2000
Mesalamine12651-582PowderBulk ingredientsMarch 21, 1988

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.