Skip to the page

Data / Drug companies / Ipg Pharmaceuticals, Inc.

Ipg Pharmaceuticals, Inc.: 12 products in the FDA NDC directory, labeler code 71085

Ipg Pharmaceuticals, Inc. (labeler code 71085) lists 12 products in the FDA National Drug Code Directory, covering 11 finished drugs by generic name. By type: 10 prescription drugs, 2 over the counter drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on September 10, 2026.

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
71085
Products in commercial distribution
12
Packages
14
Finished drugs by generic name
11
Prescription products
10
Over the counter products
2
Flagged as original packager
6 of 6 products that carry the flag
Started marketing in the last 12 months
8
Products with a marketing end date set
1
Earliest marketing start
January 13, 2025
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)975%
New drug applications (NDA)216.7%
Over the counter monograph drugs18.3%

Products by type

TypeProductsShare
Prescription drugs1083.3%
Over the counter drugs216.7%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet433.3%
Cream325%
Solution216.7%
For solution18.3%
Gel18.3%
Spray, metered18.3%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Ketoconazole71085-008CreamGeneric drugs (ANDA)September 10, 2026
Diclofenac sodium71085-084GelGeneric drugs (ANDA)September 6, 2026
Tofacitinib71085-099SolutionGeneric drugs (ANDA)June 15, 2026
Buspirone Hydrochloride71085-094TabletGeneric drugs (ANDA)May 29, 2026
Buspirone Hydrochloride71085-093TabletGeneric drugs (ANDA)May 29, 2026
Pliaglis71085-100CreamNew drug applications (NDA)March 6, 2026
Fluticasone Propionate71085-090Spray, meteredGeneric drugs (ANDA)March 6, 2026
Potassium Chloride71085-083For solutionNew drug applications (NDA)December 1, 2025
Lurbiro71085-082TabletGeneric drugs (ANDA)August 1, 2025
Clemsza71085-081TabletGeneric drugs (ANDA)August 1, 2025
Carbzah71085-080SolutionGeneric drugs (ANDA)June 1, 2025
Lidocaine Cream, 4%71085-075CreamOver the counter monograph drugsJanuary 13, 2025

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