50090-2584-0 |
50090-2584 |
HUMAN PRESCRIPTION DRUG |
Bupropion Hydrochloride SR |
bupropion hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20161102 |
N/A |
ANDA |
ANDA079095 |
A-S Medication Solutions |
BUPROPION HYDROCHLORIDE |
100 mg/1 |
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-2584-0) |
53002-1345-6 |
53002-1345 |
HUMAN PRESCRIPTION DRUG |
Bupropion Hydrochloride SR |
bupropion hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20170901 |
N/A |
ANDA |
ANDA079095 |
RPK Pharmaceuticals, Inc. |
BUPROPION HYDROCHLORIDE |
150 mg/1 |
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53002-1345-6) |
53002-1345-3 |
53002-1345 |
HUMAN PRESCRIPTION DRUG |
Bupropion Hydrochloride SR |
bupropion hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20170901 |
N/A |
ANDA |
ANDA079095 |
RPK Pharmaceuticals, Inc. |
BUPROPION HYDROCHLORIDE |
150 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53002-1345-3) |
53002-1345-0 |
53002-1345 |
HUMAN PRESCRIPTION DRUG |
Bupropion Hydrochloride SR |
bupropion hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20170901 |
N/A |
ANDA |
ANDA079095 |
RPK Pharmaceuticals, Inc. |
BUPROPION HYDROCHLORIDE |
150 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53002-1345-0) |
63187-566-30 |
63187-566 |
HUMAN PRESCRIPTION DRUG |
Bupropion Hydrochloride SR |
bupropion hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20181201 |
N/A |
ANDA |
ANDA079095 |
Proficient Rx LP |
BUPROPION HYDROCHLORIDE |
200 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-566-30) |
63187-566-60 |
63187-566 |
HUMAN PRESCRIPTION DRUG |
Bupropion Hydrochloride SR |
bupropion hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20181201 |
N/A |
ANDA |
ANDA079095 |
Proficient Rx LP |
BUPROPION HYDROCHLORIDE |
200 mg/1 |
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-566-60) |
63187-566-90 |
63187-566 |
HUMAN PRESCRIPTION DRUG |
Bupropion Hydrochloride SR |
bupropion hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20181201 |
N/A |
ANDA |
ANDA079095 |
Proficient Rx LP |
BUPROPION HYDROCHLORIDE |
200 mg/1 |
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-566-90) |
53002-2509-6 |
53002-2509 |
HUMAN PRESCRIPTION DRUG |
Bupropion Hydrochloride SR |
bupropion hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20190101 |
N/A |
ANDA |
ANDA079095 |
RPK Pharmaceuticals, Inc. |
BUPROPION HYDROCHLORIDE |
100 mg/1 |
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53002-2509-6) |
53002-2509-3 |
53002-2509 |
HUMAN PRESCRIPTION DRUG |
Bupropion Hydrochloride SR |
bupropion hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20190101 |
N/A |
ANDA |
ANDA079095 |
RPK Pharmaceuticals, Inc. |
BUPROPION HYDROCHLORIDE |
100 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53002-2509-3) |
63187-726-90 |
63187-726 |
HUMAN PRESCRIPTION DRUG |
Bupropion Hydrochloride SR |
bupropion hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20160701 |
N/A |
ANDA |
ANDA079095 |
Proficient Rx LP |
BUPROPION HYDROCHLORIDE |
150 mg/1 |
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-726-90) |
63187-726-30 |
63187-726 |
HUMAN PRESCRIPTION DRUG |
Bupropion Hydrochloride SR |
bupropion hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20160701 |
N/A |
ANDA |
ANDA079095 |
Proficient Rx LP |
BUPROPION HYDROCHLORIDE |
150 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-726-30) |
63187-726-60 |
63187-726 |
HUMAN PRESCRIPTION DRUG |
Bupropion Hydrochloride SR |
bupropion hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20160701 |
N/A |
ANDA |
ANDA079095 |
Proficient Rx LP |
BUPROPION HYDROCHLORIDE |
150 mg/1 |
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-726-60) |
63187-952-30 |
63187-952 |
HUMAN PRESCRIPTION DRUG |
Bupropion Hydrochloride SR |
bupropion hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20180101 |
N/A |
ANDA |
ANDA079095 |
Proficient Rx LP |
BUPROPION HYDROCHLORIDE |
100 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-952-30) |
63187-952-60 |
63187-952 |
HUMAN PRESCRIPTION DRUG |
Bupropion Hydrochloride SR |
bupropion hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20180101 |
N/A |
ANDA |
ANDA079095 |
Proficient Rx LP |
BUPROPION HYDROCHLORIDE |
100 mg/1 |
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-952-60) |
63187-952-90 |
63187-952 |
HUMAN PRESCRIPTION DRUG |
Bupropion Hydrochloride SR |
bupropion hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20180101 |
N/A |
ANDA |
ANDA079095 |
Proficient Rx LP |
BUPROPION HYDROCHLORIDE |
100 mg/1 |
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-952-90) |
68084-697-01 |
68084-697 |
HUMAN PRESCRIPTION DRUG |
BuPROPion Hydrochloride |
bupropion hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20150401 |
N/A |
ANDA |
ANDA079095 |
American Health Packaging |
BUPROPION HYDROCHLORIDE |
100 mg/1 |
100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-697-01) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-697-11) |
68084-708-25 |
68084-708 |
HUMAN PRESCRIPTION DRUG |
BuPROPion Hydrochloride |
bupropion hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20150401 |
N/A |
ANDA |
ANDA079095 |
American Health Packaging |
BUPROPION HYDROCHLORIDE |
150 mg/1 |
30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-708-25) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-708-95) |
70518-2029-0 |
70518-2029 |
HUMAN PRESCRIPTION DRUG |
Bupropion Hydrochloride SR |
bupropion hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20190418 |
N/A |
ANDA |
ANDA079095 |
REMEDYREPACK INC. |
BUPROPION HYDROCHLORIDE |
100 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-2029-0) |
0591-3540-60 |
0591-3540 |
HUMAN PRESCRIPTION DRUG |
Bupropion Hydrochloride SR |
bupropion hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20090702 |
N/A |
ANDA |
ANDA079095 |
Actavis Pharma, Inc. |
BUPROPION HYDROCHLORIDE |
100 mg/1 |
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0591-3540-60) |
0591-3541-60 |
0591-3541 |
HUMAN PRESCRIPTION DRUG |
Bupropion Hydrochloride SR |
bupropion hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20090702 |
N/A |
ANDA |
ANDA079095 |
Actavis Pharma, Inc. |
BUPROPION HYDROCHLORIDE |
150 mg/1 |
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0591-3541-60) |