| 51655-275-26 |
51655-275 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20200616 |
N/A |
ANDA |
ANDA090796 |
Northwind Health Company, LLC |
IBUPROFEN |
800 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-26) |
| 51655-275-54 |
51655-275 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20200921 |
N/A |
ANDA |
ANDA090796 |
Northwind Health Company, LLC |
IBUPROFEN |
800 mg/1 |
15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-54) |
| 73086-211-01 |
73086-211 |
HUMAN PRESCRIPTION DRUG |
ibuprofen |
ibuprofen |
TABLET |
ORAL |
20240320 |
N/A |
ANDA |
ANDA090796 |
SKYA HEALTH, LLC |
IBUPROFEN |
600 mg/1 |
100 TABLET in 1 BOTTLE (73086-211-01) |
| 49483-602-50 |
49483-602 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20151230 |
N/A |
ANDA |
ANDA090796 |
TIME CAP LABORATORIES, INC |
IBUPROFEN |
400 mg/1 |
500 TABLET, FILM COATED in 1 BOTTLE (49483-602-50) |
| 60760-603-30 |
60760-603 |
HUMAN PRESCRIPTION DRUG |
IBUPROFEN |
IBUPROFEN |
TABLET, FILM COATED |
ORAL |
20211020 |
N/A |
ANDA |
ANDA090796 |
St. Mary's Medical Park Pharmacy |
IBUPROFEN |
600 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-603-30) |
| 60760-603-40 |
60760-603 |
HUMAN PRESCRIPTION DRUG |
IBUPROFEN |
IBUPROFEN |
TABLET, FILM COATED |
ORAL |
20191226 |
N/A |
ANDA |
ANDA090796 |
St. Mary's Medical Park Pharmacy |
IBUPROFEN |
600 mg/1 |
40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-603-40) |
| 60760-603-60 |
60760-603 |
HUMAN PRESCRIPTION DRUG |
IBUPROFEN |
IBUPROFEN |
TABLET, FILM COATED |
ORAL |
20191021 |
N/A |
ANDA |
ANDA090796 |
St. Mary's Medical Park Pharmacy |
IBUPROFEN |
600 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-603-60) |
| 60760-603-90 |
60760-603 |
HUMAN PRESCRIPTION DRUG |
IBUPROFEN |
IBUPROFEN |
TABLET, FILM COATED |
ORAL |
20230206 |
N/A |
ANDA |
ANDA090796 |
St. Mary's Medical Park Pharmacy |
IBUPROFEN |
600 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-603-90) |
| 60760-604-09 |
60760-604 |
HUMAN PRESCRIPTION DRUG |
IBUPROFEN |
IBUPROFEN |
TABLET, FILM COATED |
ORAL |
20200610 |
N/A |
ANDA |
ANDA090796 |
St. Mary's Medical Park Pharmacy |
IBUPROFEN |
800 mg/1 |
9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-604-09) |
| 60760-604-20 |
60760-604 |
HUMAN PRESCRIPTION DRUG |
IBUPROFEN |
IBUPROFEN |
TABLET, FILM COATED |
ORAL |
20191016 |
N/A |
ANDA |
ANDA090796 |
St. Mary's Medical Park Pharmacy |
IBUPROFEN |
800 mg/1 |
20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-604-20) |
| 43063-867-01 |
43063-867 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20180711 |
N/A |
ANDA |
ANDA090796 |
PD-Rx Pharmaceuticals, Inc. |
IBUPROFEN |
600 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-867-01) |
| 43063-867-10 |
43063-867 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20180905 |
N/A |
ANDA |
ANDA090796 |
PD-Rx Pharmaceuticals, Inc. |
IBUPROFEN |
600 mg/1 |
10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-867-10) |
| 43063-867-30 |
43063-867 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20231030 |
N/A |
ANDA |
ANDA090796 |
PD-Rx Pharmaceuticals, Inc. |
IBUPROFEN |
600 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-867-30) |
| 68071-3362-2 |
68071-3362 |
HUMAN PRESCRIPTION DRUG |
IBUPROFEN |
IBUPROFEN |
TABLET, FILM COATED |
ORAL |
20170726 |
N/A |
ANDA |
ANDA090796 |
NuCare Pharmaceuticals,Inc. |
IBUPROFEN |
800 mg/1 |
20 TABLET, FILM COATED in 1 BOTTLE (68071-3362-2) |
| 68071-3362-3 |
68071-3362 |
HUMAN PRESCRIPTION DRUG |
IBUPROFEN |
IBUPROFEN |
TABLET, FILM COATED |
ORAL |
20170726 |
N/A |
ANDA |
ANDA090796 |
NuCare Pharmaceuticals,Inc. |
IBUPROFEN |
800 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (68071-3362-3) |
| 68071-3362-4 |
68071-3362 |
HUMAN PRESCRIPTION DRUG |
IBUPROFEN |
IBUPROFEN |
TABLET, FILM COATED |
ORAL |
20170726 |
N/A |
ANDA |
ANDA090796 |
NuCare Pharmaceuticals,Inc. |
IBUPROFEN |
800 mg/1 |
40 TABLET, FILM COATED in 1 BOTTLE (68071-3362-4) |
| 68071-3362-5 |
68071-3362 |
HUMAN PRESCRIPTION DRUG |
IBUPROFEN |
IBUPROFEN |
TABLET, FILM COATED |
ORAL |
20170726 |
N/A |
ANDA |
ANDA090796 |
NuCare Pharmaceuticals,Inc. |
IBUPROFEN |
800 mg/1 |
15 TABLET, FILM COATED in 1 BOTTLE (68071-3362-5) |
| 68071-3362-6 |
68071-3362 |
HUMAN PRESCRIPTION DRUG |
IBUPROFEN |
IBUPROFEN |
TABLET, FILM COATED |
ORAL |
20170726 |
N/A |
ANDA |
ANDA090796 |
NuCare Pharmaceuticals,Inc. |
IBUPROFEN |
800 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (68071-3362-6) |
| 68071-3362-9 |
68071-3362 |
HUMAN PRESCRIPTION DRUG |
IBUPROFEN |
IBUPROFEN |
TABLET, FILM COATED |
ORAL |
20170726 |
N/A |
ANDA |
ANDA090796 |
NuCare Pharmaceuticals,Inc. |
IBUPROFEN |
800 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (68071-3362-9) |
| 72189-324-30 |
72189-324 |
HUMAN PRESCRIPTION DRUG |
IBUPROFEN |
IBUPROFEN |
TABLET, FILM COATED |
ORAL |
20220221 |
N/A |
ANDA |
ANDA090796 |
Direct Rx |
IBUPROFEN |
400 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (72189-324-30) |