60505-0097-1 |
60505-0097 |
HUMAN PRESCRIPTION DRUG |
PAROXETINE |
paroxetine hydrochloride |
TABLET, FILM COATED |
ORAL |
20030908 |
N/A |
ANDA |
ANDA075356 |
Apotex Corp. |
PAROXETINE HYDROCHLORIDE ANHYDROUS |
10 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (60505-0097-1) |
60505-0097-2 |
60505-0097 |
HUMAN PRESCRIPTION DRUG |
PAROXETINE |
paroxetine hydrochloride |
TABLET, FILM COATED |
ORAL |
20030908 |
N/A |
ANDA |
ANDA075356 |
Apotex Corp. |
PAROXETINE HYDROCHLORIDE ANHYDROUS |
10 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (60505-0097-2) |
60505-0097-4 |
60505-0097 |
HUMAN PRESCRIPTION DRUG |
PAROXETINE |
paroxetine hydrochloride |
TABLET, FILM COATED |
ORAL |
20030908 |
N/A |
ANDA |
ANDA075356 |
Apotex Corp. |
PAROXETINE HYDROCHLORIDE ANHYDROUS |
10 mg/1 |
1000 TABLET, FILM COATED in 1 BOTTLE (60505-0097-4) |
60505-0101-1 |
60505-0101 |
HUMAN PRESCRIPTION DRUG |
PAROXETINE |
paroxetine hydrochloride |
TABLET, FILM COATED |
ORAL |
20030908 |
N/A |
ANDA |
ANDA075356 |
Apotex Corp. |
PAROXETINE HYDROCHLORIDE ANHYDROUS |
40 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (60505-0101-1) |
60505-0101-2 |
60505-0101 |
HUMAN PRESCRIPTION DRUG |
PAROXETINE |
paroxetine hydrochloride |
TABLET, FILM COATED |
ORAL |
20030908 |
N/A |
ANDA |
ANDA075356 |
Apotex Corp. |
PAROXETINE HYDROCHLORIDE ANHYDROUS |
40 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (60505-0101-2) |
60505-0101-4 |
60505-0101 |
HUMAN PRESCRIPTION DRUG |
PAROXETINE |
paroxetine hydrochloride |
TABLET, FILM COATED |
ORAL |
20030908 |
N/A |
ANDA |
ANDA075356 |
Apotex Corp. |
PAROXETINE HYDROCHLORIDE ANHYDROUS |
40 mg/1 |
1000 TABLET, FILM COATED in 1 BOTTLE (60505-0101-4) |
60505-0083-4 |
60505-0083 |
HUMAN PRESCRIPTION DRUG |
PAROXETINE |
paroxetine hydrochloride |
TABLET, FILM COATED |
ORAL |
20030908 |
N/A |
ANDA |
ANDA075356 |
Apotex Corp. |
PAROXETINE HYDROCHLORIDE ANHYDROUS |
20 mg/1 |
1000 TABLET, FILM COATED in 1 BOTTLE (60505-0083-4) |
60505-0084-1 |
60505-0084 |
HUMAN PRESCRIPTION DRUG |
PAROXETINE |
paroxetine hydrochloride |
TABLET, FILM COATED |
ORAL |
20030908 |
N/A |
ANDA |
ANDA075356 |
Apotex Corp. |
PAROXETINE HYDROCHLORIDE ANHYDROUS |
30 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (60505-0084-1) |
55154-7999-0 |
55154-7999 |
HUMAN PRESCRIPTION DRUG |
PAROXETINE |
paroxetine hydrochloride |
TABLET, FILM COATED |
ORAL |
20030908 |
N/A |
ANDA |
ANDA075356 |
Cardinal Health 107, LLC |
PAROXETINE HYDROCHLORIDE ANHYDROUS |
20 mg/1 |
1 BLISTER PACK in 1 BAG (55154-7999-0) / 10 TABLET, FILM COATED in 1 BLISTER PACK |
60505-0083-1 |
60505-0083 |
HUMAN PRESCRIPTION DRUG |
PAROXETINE |
paroxetine hydrochloride |
TABLET, FILM COATED |
ORAL |
20030908 |
N/A |
ANDA |
ANDA075356 |
Apotex Corp. |
PAROXETINE HYDROCHLORIDE ANHYDROUS |
20 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (60505-0083-1) |
70518-0993-1 |
70518-0993 |
HUMAN PRESCRIPTION DRUG |
PAROXETINE |
paroxetine hydrochloride |
TABLET, FILM COATED |
ORAL |
20200908 |
N/A |
ANDA |
ANDA075356 |
REMEDYREPACK INC. |
PAROXETINE HYDROCHLORIDE ANHYDROUS |
40 mg/1 |
100 POUCH in 1 BOX (70518-0993-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-0993-2) |
70518-2871-0 |
70518-2871 |
HUMAN PRESCRIPTION DRUG |
PAROXETINE |
paroxetine hydrochloride |
TABLET, FILM COATED |
ORAL |
20200908 |
N/A |
ANDA |
ANDA075356 |
REMEDYREPACK INC. |
PAROXETINE HYDROCHLORIDE ANHYDROUS |
20 mg/1 |
100 POUCH in 1 BOX (70518-2871-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-2871-1) |
61919-322-30 |
61919-322 |
HUMAN PRESCRIPTION DRUG |
PAROXETINE |
PAROXETINE |
TABLET, FILM COATED |
ORAL |
20150101 |
N/A |
ANDA |
ANDA075356 |
DIRECT RX |
PAROXETINE HYDROCHLORIDE ANHYDROUS |
10 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (61919-322-30) |
0904-5676-61 |
0904-5676 |
HUMAN PRESCRIPTION DRUG |
PAROXETINE |
paroxetine hydrochloride |
TABLET, FILM COATED |
ORAL |
20030908 |
N/A |
ANDA |
ANDA075356 |
Major Pharmaceuticals |
PAROXETINE HYDROCHLORIDE ANHYDROUS |
10 mg/1 |
100 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-5676-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK |
0904-5677-61 |
0904-5677 |
HUMAN PRESCRIPTION DRUG |
PAROXETINE |
paroxetine hydrochloride |
TABLET, FILM COATED |
ORAL |
20030908 |
N/A |
ANDA |
ANDA075356 |
Major Pharmaceuticals |
PAROXETINE HYDROCHLORIDE ANHYDROUS |
20 mg/1 |
100 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-5677-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK |
70518-0964-1 |
70518-0964 |
HUMAN PRESCRIPTION DRUG |
PAROXETINE |
paroxetine hydrochloride |
TABLET, FILM COATED |
ORAL |
20230920 |
N/A |
ANDA |
ANDA075356 |
REMEDYREPACK INC. |
PAROXETINE HYDROCHLORIDE ANHYDROUS |
10 mg/1 |
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0964-1) |
70518-1460-1 |
70518-1460 |
HUMAN PRESCRIPTION DRUG |
PAROXETINE |
paroxetine hydrochloride |
TABLET, FILM COATED |
ORAL |
20201109 |
N/A |
ANDA |
ANDA075356 |
REMEDYREPACK INC. |
PAROXETINE HYDROCHLORIDE ANHYDROUS |
30 mg/1 |
100 POUCH in 1 BOX (70518-1460-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-1460-2) |
70518-1460-0 |
70518-1460 |
HUMAN PRESCRIPTION DRUG |
PAROXETINE |
paroxetine hydrochloride |
TABLET, FILM COATED |
ORAL |
20181004 |
N/A |
ANDA |
ANDA075356 |
REMEDYREPACK INC. |
PAROXETINE HYDROCHLORIDE ANHYDROUS |
30 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1460-0) |