69844-009-01 |
69844-009 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate film coated |
fenofibrate |
TABLET |
ORAL |
20180817 |
N/A |
ANDA |
ANDA210606 |
Graviti Pharmaceuticals Private Limited |
FENOFIBRATE |
160 mg/1 |
30 TABLET in 1 BOTTLE (69844-009-01) |
69844-009-02 |
69844-009 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate film coated |
fenofibrate |
TABLET |
ORAL |
20180817 |
N/A |
ANDA |
ANDA210606 |
Graviti Pharmaceuticals Private Limited |
FENOFIBRATE |
160 mg/1 |
90 TABLET in 1 BOTTLE (69844-009-02) |
69844-009-03 |
69844-009 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate film coated |
fenofibrate |
TABLET |
ORAL |
20180817 |
N/A |
ANDA |
ANDA210606 |
Graviti Pharmaceuticals Private Limited |
FENOFIBRATE |
160 mg/1 |
1000 TABLET in 1 BOTTLE (69844-009-03) |
69844-008-03 |
69844-008 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate film coated |
fenofibrate |
TABLET |
ORAL |
20180817 |
N/A |
ANDA |
ANDA210606 |
Graviti Pharmaceuticals Private Limited |
FENOFIBRATE |
54 mg/1 |
1000 TABLET in 1 BOTTLE (69844-008-03) |
69844-008-02 |
69844-008 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate film coated |
fenofibrate |
TABLET |
ORAL |
20180817 |
N/A |
ANDA |
ANDA210606 |
Graviti Pharmaceuticals Private Limited |
FENOFIBRATE |
54 mg/1 |
90 TABLET in 1 BOTTLE (69844-008-02) |
69844-008-01 |
69844-008 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate film coated |
fenofibrate |
TABLET |
ORAL |
20180817 |
N/A |
ANDA |
ANDA210606 |
Graviti Pharmaceuticals Private Limited |
FENOFIBRATE |
54 mg/1 |
30 TABLET in 1 BOTTLE (69844-008-01) |
42385-935-05 |
42385-935 |
HUMAN PRESCRIPTION DRUG |
FENOFIBRATE |
FENOFIBRATE |
TABLET, FILM COATED |
ORAL |
20200113 |
N/A |
ANDA |
ANDA210606 |
Laurus Labs Limited |
FENOFIBRATE |
54 mg/1 |
500 TABLET, FILM COATED in 1 BOTTLE (42385-935-05) |
42385-936-05 |
42385-936 |
HUMAN PRESCRIPTION DRUG |
FENOFIBRATE |
FENOFIBRATE |
TABLET, FILM COATED |
ORAL |
20200113 |
N/A |
ANDA |
ANDA210606 |
Laurus Labs Limited |
FENOFIBRATE |
160 mg/1 |
500 TABLET, FILM COATED in 1 BOTTLE (42385-936-05) |
42385-936-11 |
42385-936 |
HUMAN PRESCRIPTION DRUG |
FENOFIBRATE |
FENOFIBRATE |
TABLET, FILM COATED |
ORAL |
20200113 |
N/A |
ANDA |
ANDA210606 |
Laurus Labs Limited |
FENOFIBRATE |
160 mg/1 |
1000 TABLET, FILM COATED in 1 BOTTLE (42385-936-11) |
42385-936-30 |
42385-936 |
HUMAN PRESCRIPTION DRUG |
FENOFIBRATE |
FENOFIBRATE |
TABLET, FILM COATED |
ORAL |
20200113 |
N/A |
ANDA |
ANDA210606 |
Laurus Labs Limited |
FENOFIBRATE |
160 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (42385-936-30) |
42385-936-90 |
42385-936 |
HUMAN PRESCRIPTION DRUG |
FENOFIBRATE |
FENOFIBRATE |
TABLET, FILM COATED |
ORAL |
20200113 |
N/A |
ANDA |
ANDA210606 |
Laurus Labs Limited |
FENOFIBRATE |
160 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (42385-936-90) |
42385-935-11 |
42385-935 |
HUMAN PRESCRIPTION DRUG |
FENOFIBRATE |
FENOFIBRATE |
TABLET, FILM COATED |
ORAL |
20200113 |
N/A |
ANDA |
ANDA210606 |
Laurus Labs Limited |
FENOFIBRATE |
54 mg/1 |
1000 TABLET, FILM COATED in 1 BOTTLE (42385-935-11) |
42385-935-30 |
42385-935 |
HUMAN PRESCRIPTION DRUG |
FENOFIBRATE |
FENOFIBRATE |
TABLET, FILM COATED |
ORAL |
20200113 |
N/A |
ANDA |
ANDA210606 |
Laurus Labs Limited |
FENOFIBRATE |
54 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (42385-935-30) |
42385-935-90 |
42385-935 |
HUMAN PRESCRIPTION DRUG |
FENOFIBRATE |
FENOFIBRATE |
TABLET, FILM COATED |
ORAL |
20200113 |
N/A |
ANDA |
ANDA210606 |
Laurus Labs Limited |
FENOFIBRATE |
54 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (42385-935-90) |
69315-289-09 |
69315-289 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate |
Fenofibrate |
TABLET, FILM COATED |
ORAL |
20220820 |
N/A |
ANDA |
ANDA210606 |
Leading Pharma, LLC |
FENOFIBRATE |
54 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (69315-289-09) |
69315-290-05 |
69315-290 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate |
Fenofibrate |
TABLET, FILM COATED |
ORAL |
20220820 |
N/A |
ANDA |
ANDA210606 |
Leading Pharma, LLC |
FENOFIBRATE |
160 mg/1 |
500 TABLET, FILM COATED in 1 BOTTLE (69315-290-05) |
69315-290-09 |
69315-290 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate |
Fenofibrate |
TABLET, FILM COATED |
ORAL |
20220820 |
N/A |
ANDA |
ANDA210606 |
Leading Pharma, LLC |
FENOFIBRATE |
160 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (69315-290-09) |