TY  - GEN
AB  - Application Number:  19-839/S-045 20-990/S-011 ; Brand name:  Zoloft
AU  - United States. Food and Drug Administration.
DA  - 2003-01-01
DO  - 10.6083/M4RR1XB8
DO  - DOI
ID  - 3324
L1  - https://digitalcollections.ohsu.edu/record/3324/files/fdadrug_45.pdf
L1  - https://digitalcollections.ohsu.edu/record/3324/files/fdadrug_thumbnail.jpg
L2  - https://digitalcollections.ohsu.edu/record/3324/files/fdadrug_45.pdf
L2  - https://digitalcollections.ohsu.edu/record/3324/files/fdadrug_thumbnail.jpg
L4  - https://digitalcollections.ohsu.edu/record/3324/files/fdadrug_45.pdf
L4  - https://digitalcollections.ohsu.edu/record/3324/files/fdadrug_thumbnail.jpg
LK  - https://digitalcollections.ohsu.edu/record/3324/files/fdadrug_45.pdf
LK  - https://digitalcollections.ohsu.edu/record/3324/files/fdadrug_thumbnail.jpg
N2  - Application Number:  19-839/S-045 20-990/S-011 ; Brand name:  Zoloft
PY  - 2003-01-01
T1  - Sertraline hydrochloride
TI  - Sertraline hydrochloride
UR  - https://digitalcollections.ohsu.edu/record/3324/files/fdadrug_45.pdf
UR  - https://digitalcollections.ohsu.edu/record/3324/files/fdadrug_thumbnail.jpg
Y1  - 2003-01-01
ER  -