000 01344 a2200445 4500
005 20250514021918.0
264 0 _c20020806
008 200208s 0 0 eng d
022 _a0724-8741
024 7 _a10.1023/a:1013319408893
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aChen, M L
245 0 0 _aBioavailability and bioequivalence: an FDA regulatory overview.
_h[electronic resource]
260 _bPharmaceutical research
_cDec 2001
300 _a1645-50 p.
_bdigital
500 _aPublication Type: Journal Article; Review
650 0 4 _aBiological Availability
650 0 4 _aDrug Approval
650 0 4 _aDrugs, Generic
650 0 4 _aDrugs, Investigational
650 0 4 _aLegislation, Drug
650 0 4 _aTherapeutic Equivalency
650 0 4 _aUnited States
650 0 4 _aUnited States Food and Drug Administration
700 1 _aShah, V
700 1 _aPatnaik, R
700 1 _aAdams, W
700 1 _aHussain, A
700 1 _aConner, D
700 1 _aMehta, M
700 1 _aMalinowski, H
700 1 _aLazor, J
700 1 _aHuang, S M
700 1 _aHare, D
700 1 _aLesko, L
700 1 _aSporn, D
700 1 _aWilliams, R
773 0 _tPharmaceutical research
_gvol. 18
_gno. 12
_gp. 1645-50
856 4 0 _uhttps://doi.org/10.1023/a:1013319408893
_zAvailable from publisher's website
999 _c11697189
_d11697189