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WARNING LETTER
•Randek l-warez

FDA WARNING_LETTER - Randek l-warez

Record Details

The FDA issued a Warning Letter to thewomantour.com for offering violative drug products for sale, including "Xanax (Generic)," "Valium (Generic)," "Viagra (Brand)," "Acomplia (Brand)," "Acomplia (Generic)," "Rimonabant," and "Herbal Ambien." The FDA determined these products are drugs under section 201(g) of the Act, intended for disease treatment or to affect body structure/function.

The firm is in violation of the Federal Food, Drug, and Cosmetic Act due to: 1. **Unapproved New Drugs:** Products like "Acomplia (Brand/Generic)," "Rimonabant," and "Herbal Ambien" are unapproved new drugs. Rimonabant (Acomplia) was specifically rejected by the FDA due to safety concerns (neurological/psychiatric side effects). "Herbal Ambien" is also considered an unapproved new drug. Introducing these into interstate commerce without FDA-approved applications violates sections 301(d) and 505(a) of the Act. 2. **Misbranded Drugs:** * Selling prescription drugs such as "Xanax (Generic)," "Valium (Generic)," and "Viagra (Brand)" without requiring a prescription from a licensed practitioner violates section 503(b)(1) and sections 301(a

Company
Randek l-warez
Product type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Deborah M. Autor (Former FDA Deputy Commissioner)
View Company Profile

ID · 596d53dd-b607-4195-b3bf-0dbaf0778ae6

Violation Codes9
21 U.S.C. 353(b)(1)21 U.S.C. 321(g)21 U.S.C. 331(a)21 U.S.C. 321(p)21 U.S.C. 331(d)21.U.S.C. 355(a)21 U.S.C. 331(b)21 U.S.C. 331(k)21 U.S.C. 352(a)

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