Main > PHARMA. > Generic Drug > USA Legislation > 1984. Hatch-Waxman Law > ANDA (Abbrev) offer 4 Market. Route > Paragraph I Certification

Product USA. Uft

METHOD - Required patent information on brand drug has not been filed.
- FDA may approve ANDA immediately, one or more generics may enter
UPDATE 09.02
COMPANY This data is not available for free
LITERATURE REF. This data is not available for free

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