68382-385-06 |
68382-385 |
HUMAN PRESCRIPTION DRUG |
Duloxetine |
Duloxetine |
CAPSULE, DELAYED RELEASE |
ORAL |
20140527 |
N/A |
ANDA |
ANDA090739 |
Zydus Pharmaceuticals (USA) Inc. |
DULOXETINE HYDROCHLORIDE |
20 mg/1 |
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-385-06) |
68382-385-14 |
68382-385 |
HUMAN PRESCRIPTION DRUG |
Duloxetine |
Duloxetine |
CAPSULE, DELAYED RELEASE |
ORAL |
20140527 |
N/A |
ANDA |
ANDA090739 |
Zydus Pharmaceuticals (USA) Inc. |
DULOXETINE HYDROCHLORIDE |
20 mg/1 |
60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-385-14) |
68382-385-16 |
68382-385 |
HUMAN PRESCRIPTION DRUG |
Duloxetine |
Duloxetine |
CAPSULE, DELAYED RELEASE |
ORAL |
20140527 |
N/A |
ANDA |
ANDA090739 |
Zydus Pharmaceuticals (USA) Inc. |
DULOXETINE HYDROCHLORIDE |
20 mg/1 |
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-385-16) |
68382-386-06 |
68382-386 |
HUMAN PRESCRIPTION DRUG |
Duloxetine |
Duloxetine |
CAPSULE, DELAYED RELEASE |
ORAL |
20140527 |
N/A |
ANDA |
ANDA090739 |
Zydus Pharmaceuticals (USA) Inc. |
DULOXETINE HYDROCHLORIDE |
30 mg/1 |
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-386-06) |
68382-386-10 |
68382-386 |
HUMAN PRESCRIPTION DRUG |
Duloxetine |
Duloxetine |
CAPSULE, DELAYED RELEASE |
ORAL |
20170406 |
N/A |
ANDA |
ANDA090739 |
Zydus Pharmaceuticals (USA) Inc. |
DULOXETINE HYDROCHLORIDE |
30 mg/1 |
1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-386-10) |
68382-386-16 |
68382-386 |
HUMAN PRESCRIPTION DRUG |
Duloxetine |
Duloxetine |
CAPSULE, DELAYED RELEASE |
ORAL |
20140527 |
N/A |
ANDA |
ANDA090739 |
Zydus Pharmaceuticals (USA) Inc. |
DULOXETINE HYDROCHLORIDE |
30 mg/1 |
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-386-16) |
68382-387-06 |
68382-387 |
HUMAN PRESCRIPTION DRUG |
Duloxetine |
Duloxetine |
CAPSULE, DELAYED RELEASE |
ORAL |
20140527 |
N/A |
ANDA |
ANDA090739 |
Zydus Pharmaceuticals (USA) Inc. |
DULOXETINE HYDROCHLORIDE |
60 mg/1 |
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-387-06) |
68382-387-10 |
68382-387 |
HUMAN PRESCRIPTION DRUG |
Duloxetine |
Duloxetine |
CAPSULE, DELAYED RELEASE |
ORAL |
20170406 |
N/A |
ANDA |
ANDA090739 |
Zydus Pharmaceuticals (USA) Inc. |
DULOXETINE HYDROCHLORIDE |
60 mg/1 |
1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-387-10) |
68382-387-16 |
68382-387 |
HUMAN PRESCRIPTION DRUG |
Duloxetine |
Duloxetine |
CAPSULE, DELAYED RELEASE |
ORAL |
20140527 |
N/A |
ANDA |
ANDA090739 |
Zydus Pharmaceuticals (USA) Inc. |
DULOXETINE HYDROCHLORIDE |
60 mg/1 |
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-387-16) |
65841-799-06 |
65841-799 |
HUMAN PRESCRIPTION DRUG |
Duloxetine |
Duloxetine |
CAPSULE, DELAYED RELEASE |
ORAL |
20140527 |
N/A |
ANDA |
ANDA090739 |
Zydus Lifesciences Limited |
DULOXETINE HYDROCHLORIDE |
20 mg/1 |
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-799-06) |
65841-799-14 |
65841-799 |
HUMAN PRESCRIPTION DRUG |
Duloxetine |
Duloxetine |
CAPSULE, DELAYED RELEASE |
ORAL |
20140527 |
N/A |
ANDA |
ANDA090739 |
Zydus Lifesciences Limited |
DULOXETINE HYDROCHLORIDE |
20 mg/1 |
60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-799-14) |
65841-799-16 |
65841-799 |
HUMAN PRESCRIPTION DRUG |
Duloxetine |
Duloxetine |
CAPSULE, DELAYED RELEASE |
ORAL |
20140527 |
N/A |
ANDA |
ANDA090739 |
Zydus Lifesciences Limited |
DULOXETINE HYDROCHLORIDE |
20 mg/1 |
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-799-16) |
65841-800-06 |
65841-800 |
HUMAN PRESCRIPTION DRUG |
Duloxetine |
Duloxetine |
CAPSULE, DELAYED RELEASE |
ORAL |
20140527 |
N/A |
ANDA |
ANDA090739 |
Zydus Lifesciences Limited |
DULOXETINE HYDROCHLORIDE |
30 mg/1 |
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-800-06) |
65841-800-10 |
65841-800 |
HUMAN PRESCRIPTION DRUG |
Duloxetine |
Duloxetine |
CAPSULE, DELAYED RELEASE |
ORAL |
20140527 |
N/A |
ANDA |
ANDA090739 |
Zydus Lifesciences Limited |
DULOXETINE HYDROCHLORIDE |
30 mg/1 |
1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-800-10) |
65841-800-16 |
65841-800 |
HUMAN PRESCRIPTION DRUG |
Duloxetine |
Duloxetine |
CAPSULE, DELAYED RELEASE |
ORAL |
20140527 |
N/A |
ANDA |
ANDA090739 |
Zydus Lifesciences Limited |
DULOXETINE HYDROCHLORIDE |
30 mg/1 |
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-800-16) |
65841-801-06 |
65841-801 |
HUMAN PRESCRIPTION DRUG |
Duloxetine |
Duloxetine |
CAPSULE, DELAYED RELEASE |
ORAL |
20140527 |
N/A |
ANDA |
ANDA090739 |
Zydus Lifesciences Limited |
DULOXETINE HYDROCHLORIDE |
60 mg/1 |
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-801-06) |
65841-801-10 |
65841-801 |
HUMAN PRESCRIPTION DRUG |
Duloxetine |
Duloxetine |
CAPSULE, DELAYED RELEASE |
ORAL |
20140527 |
N/A |
ANDA |
ANDA090739 |
Zydus Lifesciences Limited |
DULOXETINE HYDROCHLORIDE |
60 mg/1 |
1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-801-10) |
65841-801-16 |
65841-801 |
HUMAN PRESCRIPTION DRUG |
Duloxetine |
Duloxetine |
CAPSULE, DELAYED RELEASE |
ORAL |
20140527 |
N/A |
ANDA |
ANDA090739 |
Zydus Lifesciences Limited |
DULOXETINE HYDROCHLORIDE |
60 mg/1 |
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-801-16) |