Forest Laboratories, Inc.

Overview

Forest Laboratories, Inc. was a pharmaceutical company focused on the development, manufacturing, and sale of branded forms of ethical drug products, which require a physician's prescription. It is now a subsidiary of Allergan Inc. after the acquisition in 2014.

Therapeutic areas

Active pharmaceutical ingredients supplied

Substances Forest Laboratories, Inc. is evidenced to supply (US FDA Drug Master File or EU CEP). Open any ingredient to see its full supplier landscape, CAS number and patent status.

API / Drug Master Files

Forest Laboratories, Inc. holds 0 active (18 total) FDA Type II Drug Master Files — identifying it as an active-substance / API supplier. Type II DMFs are filed with the FDA to support the use of an active pharmaceutical ingredient in drug applications.

  • FACILITIES UTILIZED IN ST. LOUIS, MOInactive1989-01-03
  • SODIUM MONOFLUOROPHOSPHATE 76 MG. C.R. TABLETSInactive1987-08-28
  • FACILITIES AND PERSONNEL IN RIO PIEDRAS, PUERTO RICOInactive1987-04-28
  • THIORIDAZINE HCL. 50MG.C.R.TABLETSInactive1985-09-06
  • QUINIDINE GLUCONATE 650 MG. C.R. TABLETSInactive1985-07-01
  • ERYTHROMYCIN 500MG. C.R.TABLETSInactive1985-06-03
  • PENTAERYTHRITOL TETRANITRATE (P.E.T.N.) 80mg. & 160mg C.R. TABLETSInactive1985-05-13
  • THIORIDAZINE HCL 400MG S.R.TABS (IN SYNCHRON VEHICLE)Inactive1985-02-14
  • THIORIDAZINE HCL 200 MG C.R. TABS (IN SYNCHRON VEHICLE)Inactive1984-11-28
  • FLURBIPROFEN 200 mg C.R. TABS (IN SYNCHRON VEHICLEInactive1983-10-26
  • FLURBIPROFEN 100 MG C.R.TABS (IN SYNCHRON VEHICLEInactive1983-10-26
  • IBUPROFEN 800 MG C.R. TABLETS (IN SYNCHRON VEHICLE)Inactive1982-09-02
  • THIORIDAZINE HCL100MG CR(LD IN SYCHRON VEHICLE)MNFG INWOOD,NYInactive1982-07-27
  • THIORIDAZINE HCl C.R. TABLETS (IN SYNCHRON VEHICLE)Inactive1982-07-27
  • SODIUM FLUORIDE 22MG, SUSTAINED ACTION CAPSULESInactive1981-10-08

Showing 15 of 18 Drug Master Files.

FDA compliance signals

1 FDA enforcement record linked to this company.

  • recall — Class II2017-06-07

    Labeling; Label Mixup; blister lidding foil and shell-pack labeled as 10 mg but package actually contains 5 mg tablets

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