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Watson Pharmaceuticals, Inc., a leading specialty pharmaceutical company, announced that its subsidiary, Watson Laboratories, Inc., has received approval from the United States Food and Drug Administration on its Abbreviated New Drug Application (ANDA) for galantamine hydrobromide extended-release capsules, eq. to 8 mg, 16 mg and 24 mg (galantamine base). Galantamine hydrobromide extended-release capsules are the generic equivalent to Ortho McNeil Janssen's Razadyne ER, galantamine HBr extended-release capsules, which are indicated for the treatment of Alzheimer's disease.

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