| 51655-042-25 |
51655-042 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20220909 |
N/A |
ANDA |
ANDA091625 |
Northwind Health Company, LLC |
IBUPROFEN |
600 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-042-25) |
| 51655-042-26 |
51655-042 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20221214 |
N/A |
ANDA |
ANDA091625 |
Northwind Health Company, LLC |
IBUPROFEN |
600 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-042-26) |
| 51655-042-52 |
51655-042 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20230628 |
N/A |
ANDA |
ANDA091625 |
Northwind Health Company, LLC |
IBUPROFEN |
600 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-042-52) |
| 51655-385-20 |
51655-385 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20230220 |
N/A |
ANDA |
ANDA091625 |
Northwind Health Company, LLC |
IBUPROFEN |
800 mg/1 |
20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-385-20) |
| 51655-385-51 |
51655-385 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20200521 |
N/A |
ANDA |
ANDA091625 |
Northwind Health Company, LLC |
IBUPROFEN |
800 mg/1 |
40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-385-51) |
| 51655-385-52 |
51655-385 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20200521 |
N/A |
ANDA |
ANDA091625 |
Northwind Health Company, LLC |
IBUPROFEN |
800 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-385-52) |
| 51655-385-54 |
51655-385 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20210507 |
N/A |
ANDA |
ANDA091625 |
Northwind Health Company, LLC |
IBUPROFEN |
800 mg/1 |
15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-385-54) |
| 51655-385-21 |
51655-385 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20200521 |
N/A |
ANDA |
ANDA091625 |
Northwind Health Company, LLC |
IBUPROFEN |
800 mg/1 |
21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-385-21) |
| 51655-385-25 |
51655-385 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20230407 |
N/A |
ANDA |
ANDA091625 |
Northwind Health Company, LLC |
IBUPROFEN |
800 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-385-25) |
| 51655-385-26 |
51655-385 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20220908 |
N/A |
ANDA |
ANDA091625 |
Northwind Health Company, LLC |
IBUPROFEN |
800 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-385-26) |
| 61919-463-15 |
61919-463 |
HUMAN PRESCRIPTION DRUG |
IBUPROFEN |
IBUOROFEN |
TABLET, FILM COATED |
ORAL |
20190822 |
N/A |
ANDA |
ANDA091625 |
Direct_Rx |
IBUPROFEN |
800 mg/1 |
15 TABLET, FILM COATED in 1 BOTTLE (61919-463-15) |
| 61919-463-60 |
61919-463 |
HUMAN PRESCRIPTION DRUG |
IBUPROFEN |
IBUOROFEN |
TABLET, FILM COATED |
ORAL |
20190822 |
N/A |
ANDA |
ANDA091625 |
Direct_Rx |
IBUPROFEN |
800 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (61919-463-60) |
| 61919-463-71 |
61919-463 |
HUMAN PRESCRIPTION DRUG |
IBUPROFEN |
IBUOROFEN |
TABLET, FILM COATED |
ORAL |
20190822 |
N/A |
ANDA |
ANDA091625 |
Direct_Rx |
IBUPROFEN |
800 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (61919-463-71) |
| 61919-463-72 |
61919-463 |
HUMAN PRESCRIPTION DRUG |
IBUPROFEN |
IBUOROFEN |
TABLET, FILM COATED |
ORAL |
20190822 |
N/A |
ANDA |
ANDA091625 |
Direct_Rx |
IBUPROFEN |
800 mg/1 |
120 TABLET, FILM COATED in 1 BOTTLE (61919-463-72) |
| 61919-463-90 |
61919-463 |
HUMAN PRESCRIPTION DRUG |
IBUPROFEN |
IBUOROFEN |
TABLET, FILM COATED |
ORAL |
20190822 |
N/A |
ANDA |
ANDA091625 |
Direct_Rx |
IBUPROFEN |
800 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (61919-463-90) |
| 61919-463-21 |
61919-463 |
HUMAN PRESCRIPTION DRUG |
IBUPROFEN |
IBUOROFEN |
TABLET, FILM COATED |
ORAL |
20190822 |
N/A |
ANDA |
ANDA091625 |
Direct_Rx |
IBUPROFEN |
800 mg/1 |
21 TABLET, FILM COATED in 1 BOTTLE (61919-463-21) |
| 61919-463-40 |
61919-463 |
HUMAN PRESCRIPTION DRUG |
IBUPROFEN |
IBUOROFEN |
TABLET, FILM COATED |
ORAL |
20190822 |
N/A |
ANDA |
ANDA091625 |
Direct_Rx |
IBUPROFEN |
800 mg/1 |
40 TABLET, FILM COATED in 1 BOTTLE (61919-463-40) |
| 61919-463-45 |
61919-463 |
HUMAN PRESCRIPTION DRUG |
IBUPROFEN |
IBUOROFEN |
TABLET, FILM COATED |
ORAL |
20190822 |
N/A |
ANDA |
ANDA091625 |
Direct_Rx |
IBUPROFEN |
800 mg/1 |
45 TABLET, FILM COATED in 1 BOTTLE (61919-463-45) |
| 63187-967-15 |
63187-967 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20190801 |
N/A |
ANDA |
ANDA091625 |
Proficient Rx LP |
IBUPROFEN |
400 mg/1 |
15 TABLET, FILM COATED in 1 BOTTLE (63187-967-15) |
| 63187-967-50 |
63187-967 |
HUMAN PRESCRIPTION DRUG |
Ibuprofen |
Ibuprofen |
TABLET, FILM COATED |
ORAL |
20180101 |
N/A |
ANDA |
ANDA091625 |
Proficient Rx LP |
IBUPROFEN |
400 mg/1 |
50 TABLET, FILM COATED in 1 BOTTLE (63187-967-50) |