69986-011-01 |
69986-011 |
HUMAN PRESCRIPTION DRUG |
paroxetine hydrochloride |
paroxetine hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20231222 |
N/A |
ANDA |
ANDA213612 |
Sinotherapeutics Inc. |
PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
12.5 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69986-011-01) |
69986-011-18 |
69986-011 |
HUMAN PRESCRIPTION DRUG |
paroxetine hydrochloride |
paroxetine hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20231222 |
N/A |
ANDA |
ANDA213612 |
Sinotherapeutics Inc. |
PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
12.5 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 CARTON (69986-011-18) |
69986-012-01 |
69986-012 |
HUMAN PRESCRIPTION DRUG |
paroxetine hydrochloride |
paroxetine hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20231222 |
N/A |
ANDA |
ANDA213612 |
Sinotherapeutics Inc. |
PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
25 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69986-012-01) |
69986-012-18 |
69986-012 |
HUMAN PRESCRIPTION DRUG |
paroxetine hydrochloride |
paroxetine hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20231222 |
N/A |
ANDA |
ANDA213612 |
Sinotherapeutics Inc. |
PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
25 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 CARTON (69986-012-18) |
69986-017-01 |
69986-017 |
HUMAN PRESCRIPTION DRUG |
paroxetine hydrochloride |
paroxetine hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20231222 |
N/A |
ANDA |
ANDA213612 |
Sinotherapeutics Inc. |
PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
37.5 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69986-017-01) |