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Data / Drug companies / E. Fougera & Co. a Division of Fougera Pharmaceuticals, LLC

E. Fougera & Co. a Division of Fougera Pharmaceuticals, LLC: 38 products in the FDA NDC directory, labeler code 0168

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

E. Fougera & Co. a Division of Fougera Pharmaceuticals, LLC (labeler code 0168) lists 38 products in the FDA National Drug Code Directory, covering 18 finished drugs by generic name. By type: 37 prescription drugs, 1 over the counter drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on March 9, 2016.

The request: Watch E. Fougera & Co. a Division of Fougera Pharmaceuticals, LLC (FDA labeler code 0168): 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
0168
Products in commercial distribution
38
Packages
67
Finished drugs by generic name
18
Prescription products
37
Over the counter products
1
Flagged as original packager
37 of 37 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
April 3, 1970
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)3078.9%
New drug applications (NDA)615.8%
Over the counter monograph drugs12.6%
Authorized generics (NDA)12.6%

Products by type

TypeProductsShare
Prescription drugs3797.4%
Over the counter drugs12.6%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Cream1642.1%
Ointment1026.3%
Solution513.2%
Lotion410.5%
Ointment, augmented12.6%
Lotion, augmented12.6%
Gel12.6%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Oxiconazole Nitrate0168-0358CreamAuthorized generics (NDA)March 9, 2016
Tacrolimus0168-0417OintmentGeneric drugs (ANDA)September 9, 2014
Tacrolimus0168-0416OintmentGeneric drugs (ANDA)September 9, 2014
Adapalene0168-0424CreamGeneric drugs (ANDA)June 30, 2010
Betamethasone Dipropionate0168-0267Lotion, augmentedGeneric drugs (ANDA)May 21, 2007
Metronidazole0168-0383LotionGeneric drugs (ANDA)May 24, 2006
Terconazole0168-0346CreamGeneric drugs (ANDA)February 18, 2005
Terconazole Vaginal Cream 0.8%0168-0347CreamNew drug applications (NDA)February 1, 2005
Clindamycin Phosphate0168-0277CreamGeneric drugs (ANDA)December 27, 2004
Metronidazole0168-0323CreamGeneric drugs (ANDA)May 28, 2004
Ketoconazole0168-0099CreamGeneric drugs (ANDA)April 28, 2004
Lidocaine and Prilocaine0168-0357CreamGeneric drugs (ANDA)August 18, 2003
Clindamycin phosphate0168-0203LotionGeneric drugs (ANDA)January 31, 2002
Clotrimazole and Betamethasone Dipropionate0168-0258CreamGeneric drugs (ANDA)June 5, 2001
Clindamycin phosphate0168-0202GelGeneric drugs (ANDA)January 28, 2000
Betamethasone Dipropionate0168-0268Ointment, augmentedGeneric drugs (ANDA)June 22, 1999
Clobetasol Propionate0168-0269SolutionGeneric drugs (ANDA)February 8, 1999
Clindamycin phosphate0168-0201SolutionGeneric drugs (ANDA)June 5, 1997
Fluocinonide0168-0134SolutionGeneric drugs (ANDA)February 27, 1995
Hydrocortisone0168-0146OintmentGeneric drugs (ANDA)May 28, 1993
Hydrocortisone0168-0080CreamGeneric drugs (ANDA)December 16, 1986
Betamethasone Dipropionate0168-0057LotionGeneric drugs (ANDA)August 12, 1985
Betamethasone Dipropionate0168-0056OintmentNew drug applications (NDA)September 4, 1984
Betamethasone Dipropionate0168-0055CreamNew drug applications (NDA)June 26, 1984
Betamethasone Valerate0168-0041LotionNew drug applications (NDA)August 31, 1983

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.