Sunrise ProductsSafe and affordable generic medications for millions of patients to lead a happier and healthier life
We produce every pill, every bottle with tremendous pride and assure its safety, efficacy and affordability. Each Sunrise product is a result of state-of-the-art manufacturing technologies combined with the strictest quality control processes. As a trusted partner to pharmaceutical industry our products are manufactured with full compliance to Quality. Our constant goal is to exceed all current regulations and provide quality products to our trading partners and consumers at large.
Every employee receives training in current Good Manufacturing Practice (cGMP) and standard operating procedures (SOPs). Internal routine audits and external inspections assure that our quality systems are consistent with current GMP industry standards at all times. We understand the role of medicine and we intend to fulfill the medical, social, and ethical obligation to deliver a high quality yet affordable product.
For more details regarding our full product list please contact our Sales team.
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Generic drugs contain the same active ingredient and are identical in strength, dosage form, and route of administration, as the brand-name drug. In the United States, upon patent expiration (of the brand drug) or a successful challenge of relevant patents, a manufacturer can produce a generic drug as long as it meets FDA approval and bioequivalence standards. FDA can only approve the generic if it contains the same active ingredients as the innovator drug, be identical in strength, dosage form and route of administration, have the same use indications, be bio-equivalent.
Generic meet the same batch requirements for identity, strength, purity and quality, and be manufactured under the same strict standards of FDA‘s good manufacturing practice regulations required for innovator products. Generics are marketed under the drug’s chemical, or “generic,” name and meet the same FDA quality and effectiveness standards as the original.