Skip to the page

Data / Drug companies / Pangea Pharmaceuticals, LLC

Pangea Pharmaceuticals, LLC: 14 products in the FDA NDC directory, labeler code 81279

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

Pangea Pharmaceuticals, LLC (labeler code 81279) lists 14 products in the FDA National Drug Code Directory, covering 8 finished drugs by generic name. By type: 14 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on October 12, 2026.

The request: Watch Pangea Pharmaceuticals, LLC (FDA labeler code 81279): 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
81279
Products in commercial distribution
14
Packages
20
Finished drugs by generic name
8
Prescription products
14
Over the counter products
0
Flagged as original packager
10 of 10 products that carry the flag
Started marketing in the last 12 months
11
Earliest marketing start
May 20, 2024
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)1071.4%
New drug applications (NDA)321.4%
Other unapproved drugs17.1%

Products by type

TypeProductsShare
Prescription drugs14100%

Drugs it lists

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

DrugProductsCompanies listing it
Buspirone hydrochloride450
Amlodipine33
Dexamethasone245
Cyproheptadine hydrochloride124
Ergotamine tartrate11
Selenious acid14
Gabapentin191
Ursodiol128

Dosage forms

Dosage formProductsShare
Capsule642.9%
Tablet428.6%
Solution321.4%
Injection, solution17.1%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Cyproheptadine hydrochloride81279-129TabletGeneric drugs (ANDA)October 12, 2026
Sdamlo81279-135SolutionNew drug applications (NDA)October 2, 2026
Sdamlo81279-133SolutionNew drug applications (NDA)October 2, 2026
Ursolign81279-130CapsuleGeneric drugs (ANDA)June 15, 2026
Gabapentin81279-126CapsuleGeneric drugs (ANDA)May 22, 2026
Dexamethasone81279-117TabletGeneric drugs (ANDA)May 1, 2026
Dexamethasone81279-117TabletGeneric drugs (ANDA)May 1, 2026
Sdamlo81279-134SolutionNew drug applications (NDA)April 17, 2026
Bucapsol81279-122CapsuleGeneric drugs (ANDA)April 10, 2026
Bucapsol81279-121CapsuleGeneric drugs (ANDA)April 10, 2026
Bucapsol81279-123CapsuleGeneric drugs (ANDA)December 29, 2025
Bucapsol81279-124CapsuleGeneric drugs (ANDA)July 14, 2025
Ergomar Sublingual81279-104TabletGeneric drugs (ANDA)February 3, 2025
Selenious Acid81279-106Injection, solutionOther unapproved drugsMay 20, 2024

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.