| 82804-024-30 |
82804-024 |
HUMAN PRESCRIPTION DRUG |
Duloxetine Delayed-Release |
DULOXETINE HYDROCHLORIDE |
CAPSULE, DELAYED RELEASE PELLETS |
ORAL |
20231016 |
N/A |
ANDA |
ANDA203088 |
Proficient Rx LP |
DULOXETINE HYDROCHLORIDE |
40 mg/1 |
30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82804-024-30) |
| 82804-024-60 |
82804-024 |
HUMAN PRESCRIPTION DRUG |
Duloxetine Delayed-Release |
DULOXETINE HYDROCHLORIDE |
CAPSULE, DELAYED RELEASE PELLETS |
ORAL |
20231016 |
N/A |
ANDA |
ANDA203088 |
Proficient Rx LP |
DULOXETINE HYDROCHLORIDE |
40 mg/1 |
60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82804-024-60) |
| 82804-024-90 |
82804-024 |
HUMAN PRESCRIPTION DRUG |
Duloxetine Delayed-Release |
DULOXETINE HYDROCHLORIDE |
CAPSULE, DELAYED RELEASE PELLETS |
ORAL |
20231016 |
N/A |
ANDA |
ANDA203088 |
Proficient Rx LP |
DULOXETINE HYDROCHLORIDE |
40 mg/1 |
90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82804-024-90) |
| 51991-750-90 |
51991-750 |
HUMAN PRESCRIPTION DRUG |
Duloxetine Delayed-Release |
DULOXETINE HYDROCHLORIDE |
CAPSULE, DELAYED RELEASE PELLETS |
ORAL |
20180521 |
N/A |
ANDA |
ANDA203088 |
Breckenridge Pharmaceutical, Inc. |
DULOXETINE HYDROCHLORIDE |
40 mg/1 |
90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-750-90) |
| 51991-750-33 |
51991-750 |
HUMAN PRESCRIPTION DRUG |
Duloxetine Delayed-Release |
DULOXETINE HYDROCHLORIDE |
CAPSULE, DELAYED RELEASE PELLETS |
ORAL |
20180521 |
N/A |
ANDA |
ANDA203088 |
Breckenridge Pharmaceutical, Inc. |
DULOXETINE HYDROCHLORIDE |
40 mg/1 |
30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-750-33) |
| 51991-750-10 |
51991-750 |
HUMAN PRESCRIPTION DRUG |
Duloxetine Delayed-Release |
DULOXETINE HYDROCHLORIDE |
CAPSULE, DELAYED RELEASE PELLETS |
ORAL |
20180521 |
N/A |
ANDA |
ANDA203088 |
Breckenridge Pharmaceutical, Inc. |
DULOXETINE HYDROCHLORIDE |
40 mg/1 |
1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-750-10) |
| 51991-750-05 |
51991-750 |
HUMAN PRESCRIPTION DRUG |
Duloxetine Delayed-Release |
DULOXETINE HYDROCHLORIDE |
CAPSULE, DELAYED RELEASE PELLETS |
ORAL |
20180521 |
N/A |
ANDA |
ANDA203088 |
Breckenridge Pharmaceutical, Inc. |
DULOXETINE HYDROCHLORIDE |
40 mg/1 |
500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-750-05) |
| 71335-0165-1 |
71335-0165 |
HUMAN PRESCRIPTION DRUG |
Duloxetine Delayed-Release |
DULOXETINE HYDROCHLORIDE |
CAPSULE, DELAYED RELEASE PELLETS |
ORAL |
20180503 |
N/A |
ANDA |
ANDA203088 |
Bryant Ranch Prepack |
DULOXETINE HYDROCHLORIDE |
20 mg/1 |
30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0165-1) |
| 51991-748-10 |
51991-748 |
HUMAN PRESCRIPTION DRUG |
Duloxetine Delayed-Release |
DULOXETINE HYDROCHLORIDE |
CAPSULE, DELAYED RELEASE PELLETS |
ORAL |
20140611 |
N/A |
ANDA |
ANDA203088 |
Breckenridge Pharmaceutical, Inc. |
DULOXETINE HYDROCHLORIDE |
60 mg/1 |
1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-748-10) |
| 51991-748-33 |
51991-748 |
HUMAN PRESCRIPTION DRUG |
Duloxetine Delayed-Release |
DULOXETINE HYDROCHLORIDE |
CAPSULE, DELAYED RELEASE PELLETS |
ORAL |
20140611 |
N/A |
ANDA |
ANDA203088 |
Breckenridge Pharmaceutical, Inc. |
DULOXETINE HYDROCHLORIDE |
60 mg/1 |
30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-748-33) |
| 51991-748-90 |
51991-748 |
HUMAN PRESCRIPTION DRUG |
Duloxetine Delayed-Release |
DULOXETINE HYDROCHLORIDE |
CAPSULE, DELAYED RELEASE PELLETS |
ORAL |
20140611 |
N/A |
ANDA |
ANDA203088 |
Breckenridge Pharmaceutical, Inc. |
DULOXETINE HYDROCHLORIDE |
60 mg/1 |
90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-748-90) |
| 51991-747-10 |
51991-747 |
HUMAN PRESCRIPTION DRUG |
Duloxetine Delayed-Release |
DULOXETINE HYDROCHLORIDE |
CAPSULE, DELAYED RELEASE PELLETS |
ORAL |
20140611 |
N/A |
ANDA |
ANDA203088 |
Breckenridge Pharmaceutical, Inc. |
DULOXETINE HYDROCHLORIDE |
30 mg/1 |
1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-747-10) |
| 51991-747-33 |
51991-747 |
HUMAN PRESCRIPTION DRUG |
Duloxetine Delayed-Release |
DULOXETINE HYDROCHLORIDE |
CAPSULE, DELAYED RELEASE PELLETS |
ORAL |
20140611 |
N/A |
ANDA |
ANDA203088 |
Breckenridge Pharmaceutical, Inc. |
DULOXETINE HYDROCHLORIDE |
30 mg/1 |
30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-747-33) |
| 51991-747-90 |
51991-747 |
HUMAN PRESCRIPTION DRUG |
Duloxetine Delayed-Release |
DULOXETINE HYDROCHLORIDE |
CAPSULE, DELAYED RELEASE PELLETS |
ORAL |
20140611 |
N/A |
ANDA |
ANDA203088 |
Breckenridge Pharmaceutical, Inc. |
DULOXETINE HYDROCHLORIDE |
30 mg/1 |
90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-747-90) |
| 51991-746-05 |
51991-746 |
HUMAN PRESCRIPTION DRUG |
Duloxetine Delayed-Release |
DULOXETINE HYDROCHLORIDE |
CAPSULE, DELAYED RELEASE PELLETS |
ORAL |
20140611 |
N/A |
ANDA |
ANDA203088 |
Breckenridge Pharmaceutical, Inc. |
DULOXETINE HYDROCHLORIDE |
20 mg/1 |
500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-746-05) |
| 51991-746-06 |
51991-746 |
HUMAN PRESCRIPTION DRUG |
Duloxetine Delayed-Release |
DULOXETINE HYDROCHLORIDE |
CAPSULE, DELAYED RELEASE PELLETS |
ORAL |
20140611 |
N/A |
ANDA |
ANDA203088 |
Breckenridge Pharmaceutical, Inc. |
DULOXETINE HYDROCHLORIDE |
20 mg/1 |
60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-746-06) |
| 51991-746-90 |
51991-746 |
HUMAN PRESCRIPTION DRUG |
Duloxetine Delayed-Release |
DULOXETINE HYDROCHLORIDE |
CAPSULE, DELAYED RELEASE PELLETS |
ORAL |
20140611 |
N/A |
ANDA |
ANDA203088 |
Breckenridge Pharmaceutical, Inc. |
DULOXETINE HYDROCHLORIDE |
20 mg/1 |
90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-746-90) |
| 71335-0165-2 |
71335-0165 |
HUMAN PRESCRIPTION DRUG |
Duloxetine Delayed-Release |
DULOXETINE HYDROCHLORIDE |
CAPSULE, DELAYED RELEASE PELLETS |
ORAL |
20180712 |
N/A |
ANDA |
ANDA203088 |
Bryant Ranch Prepack |
DULOXETINE HYDROCHLORIDE |
20 mg/1 |
60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0165-2) |
| 71335-0165-3 |
71335-0165 |
HUMAN PRESCRIPTION DRUG |
Duloxetine Delayed-Release |
DULOXETINE HYDROCHLORIDE |
CAPSULE, DELAYED RELEASE PELLETS |
ORAL |
20211227 |
N/A |
ANDA |
ANDA203088 |
Bryant Ranch Prepack |
DULOXETINE HYDROCHLORIDE |
20 mg/1 |
28 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0165-3) |
| 71335-0165-4 |
71335-0165 |
HUMAN PRESCRIPTION DRUG |
Duloxetine Delayed-Release |
DULOXETINE HYDROCHLORIDE |
CAPSULE, DELAYED RELEASE PELLETS |
ORAL |
20180524 |
N/A |
ANDA |
ANDA203088 |
Bryant Ranch Prepack |
DULOXETINE HYDROCHLORIDE |
20 mg/1 |
90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0165-4) |