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Data / Drug companies / Mayne Pharma

Mayne Pharma: 26 products in the FDA NDC directory, labeler code 68308

Mayne Pharma (labeler code 68308) lists 26 products in the FDA National Drug Code Directory, covering 16 finished drugs by generic name. By type: 26 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on July 15, 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
68308
Products in commercial distribution
26
Packages
31
Finished drugs by generic name
16
Prescription products
26
Over the counter products
0
Controlled substance products
Schedule II 1
Flagged as original packager
22 of 22 products that carry the flag
Started marketing in the last 12 months
1
Earliest marketing start
April 26, 2010
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)1453.8%
Authorized generics (NDA)1038.5%
New drug applications (NDA)27.7%

Products by type

TypeProductsShare
Prescription drugs26100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Capsule, liquid filled830.8%
Gel623.1%
Cream415.4%
Aerosol, foam27.7%
Ring13.8%
Shampoo13.8%
Lotion13.8%
Tablet13.8%
Tablet, delayed release13.8%
Capsule13.8%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Rhofade68308-766CreamNew drug applications (NDA)July 15, 2026
Clindamycin Phosphate and Benzoyl Peroxide68308-127GelGeneric drugs (ANDA)October 1, 2025
Metronidazole68308-711CreamAuthorized generics (NDA)May 19, 2025
Metronidazole68308-712LotionAuthorized generics (NDA)February 10, 2025
Tretinoin (Microsphere)68308-777GelGeneric drugs (ANDA)October 25, 2024
Annovera68308-752RingNew drug applications (NDA)August 16, 2024
Adapalene68308-666GelAuthorized generics (NDA)February 26, 2024
Ivermectin68308-701CreamAuthorized generics (NDA)January 8, 2024
Halobetasol propionate68308-769Aerosol, foamGeneric drugs (ANDA)November 27, 2023
Metronidazole68308-663GelAuthorized generics (NDA)November 10, 2023
Clobetasol propionate68308-664ShampooAuthorized generics (NDA)November 3, 2023
Doxycycline68308-668CapsuleAuthorized generics (NDA)February 27, 2023
Dapsone68308-342GelGeneric drugs (ANDA)February 11, 2022
Adapalene and benzoyl peroxide68308-662GelAuthorized generics (NDA)February 1, 2022
Tazarotene68308-745CreamGeneric drugs (ANDA)November 10, 2021
Isotretinoin68308-573Capsule, liquid filledGeneric drugs (ANDA)September 21, 2021
Isotretinoin68308-571Capsule, liquid filledGeneric drugs (ANDA)September 21, 2021
Isotretinoin68308-570Capsule, liquid filledGeneric drugs (ANDA)September 21, 2021
Isotretinoin68308-575Capsule, liquid filledGeneric drugs (ANDA)September 3, 2021
Tazarotene68308-685Aerosol, foamAuthorized generics (NDA)April 23, 2021
Doxycycline Hyclate68308-716Tablet, delayed releaseAuthorized generics (NDA)February 1, 2016
Isotretinoin68308-784Capsule, liquid filledGeneric drugs (ANDA)May 1, 2012
Isotretinoin68308-783Capsule, liquid filledGeneric drugs (ANDA)May 1, 2012
Isotretinoin68308-782Capsule, liquid filledGeneric drugs (ANDA)May 1, 2012
Isotretinoin68308-781Capsule, liquid filledGeneric drugs (ANDA)May 1, 2012

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.