| 72189-266-72 |
72189-266 |
HUMAN PRESCRIPTION DRUG |
IBUPROFEN |
IBUPROFEN |
TABLET, FILM COATED |
ORAL |
20210916 |
N/A |
ANDA |
ANDA090796 |
DIRECT RX |
IBUPROFEN |
800 mg/1 |
120 TABLET, FILM COATED in 1 BOTTLE (72189-266-72) |
| 72189-266-90 |
72189-266 |
HUMAN PRESCRIPTION DRUG |
IBUPROFEN |
IBUPROFEN |
TABLET, FILM COATED |
ORAL |
20210916 |
N/A |
ANDA |
ANDA090796 |
DIRECT RX |
IBUPROFEN |
800 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (72189-266-90) |
| 25000-122-03 |
25000-122 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET |
ORAL |
20110228 |
N/A |
ANDA |
ANDA090796 |
MARKSANS PHARMA LIMITED |
IBUPROFEN |
600 mg/1 |
30 TABLET in 1 BOTTLE (25000-122-03) |
| 25000-122-12 |
25000-122 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET |
ORAL |
20110228 |
N/A |
ANDA |
ANDA090796 |
MARKSANS PHARMA LIMITED |
IBUPROFEN |
600 mg/1 |
500 TABLET in 1 BOTTLE (25000-122-12) |
| 42708-097-30 |
42708-097 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20190531 |
N/A |
ANDA |
ANDA090796 |
QPharma, Inc. |
IBUPROFEN |
600 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (42708-097-30) |
| 51655-474-20 |
51655-474 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20201119 |
N/A |
ANDA |
ANDA090796 |
Northwind Health Company, LLC |
IBUPROFEN |
600 mg/1 |
20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-474-20) |
| 51655-474-25 |
51655-474 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20201113 |
N/A |
ANDA |
ANDA090796 |
Northwind Health Company, LLC |
IBUPROFEN |
600 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-474-25) |
| 51655-474-26 |
51655-474 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20220621 |
N/A |
ANDA |
ANDA090796 |
Northwind Health Company, LLC |
IBUPROFEN |
600 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-474-26) |
| 51655-474-51 |
51655-474 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20210208 |
N/A |
ANDA |
ANDA090796 |
Northwind Health Company, LLC |
IBUPROFEN |
600 mg/1 |
40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-474-51) |
| 51655-474-52 |
51655-474 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20210114 |
N/A |
ANDA |
ANDA090796 |
Northwind Health Company, LLC |
IBUPROFEN |
600 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-474-52) |
| 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) |
| 68071-3362-0 |
68071-3362 |
HUMAN PRESCRIPTION DRUG |
IBUPROFEN |
IBUPROFEN |
TABLET, FILM COATED |
ORAL |
20170726 |
N/A |
ANDA |
ANDA090796 |
NuCare Pharmaceuticals,Inc. |
IBUPROFEN |
800 mg/1 |
12 TABLET, FILM COATED in 1 BOTTLE (68071-3362-0) |
| 68071-3362-1 |
68071-3362 |
HUMAN PRESCRIPTION DRUG |
IBUPROFEN |
IBUPROFEN |
TABLET, FILM COATED |
ORAL |
20170726 |
N/A |
ANDA |
ANDA090796 |
NuCare Pharmaceuticals,Inc. |
IBUPROFEN |
800 mg/1 |
21 TABLET, FILM COATED in 1 BOTTLE (68071-3362-1) |
| 49483-604-01 |
49483-604 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20151230 |
N/A |
ANDA |
ANDA090796 |
TIME CAP LABORATORIES, INC |
IBUPROFEN |
800 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (49483-604-01) |
| 49483-604-03 |
49483-604 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20151230 |
N/A |
ANDA |
ANDA090796 |
TIME CAP LABORATORIES, INC |
IBUPROFEN |
800 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (49483-604-03) |
| 80425-0089-1 |
80425-0089 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20151230 |
N/A |
ANDA |
ANDA090796 |
Advanced Rx of Tennessee, LLC |
IBUPROFEN |
800 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (80425-0089-1) |
| 80425-0089-2 |
80425-0089 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20151230 |
N/A |
ANDA |
ANDA090796 |
Advanced Rx of Tennessee, LLC |
IBUPROFEN |
800 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (80425-0089-2) |
| 80425-0089-3 |
80425-0089 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20151230 |
N/A |
ANDA |
ANDA090796 |
Advanced Rx of Tennessee, LLC |
IBUPROFEN |
800 mg/1 |
120 TABLET, FILM COATED in 1 BOTTLE (80425-0089-3) |
| 80425-0089-4 |
80425-0089 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20151230 |
N/A |
ANDA |
ANDA090796 |
Advanced Rx of Tennessee, LLC |
IBUPROFEN |
800 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (80425-0089-4) |