63629-1100-1 |
63629-1100 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate |
Fenofibrate |
TABLET, FILM COATED |
ORAL |
20211130 |
N/A |
ANDA |
ANDA076635 |
Bryant Ranch Prepack |
FENOFIBRATE |
54 mg/1 |
50 TABLET, FILM COATED in 1 BOTTLE (63629-1100-1) |
63629-1100-2 |
63629-1100 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate |
Fenofibrate |
TABLET, FILM COATED |
ORAL |
20211130 |
N/A |
ANDA |
ANDA076635 |
Bryant Ranch Prepack |
FENOFIBRATE |
54 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (63629-1100-2) |
43353-001-19 |
43353-001 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate |
Fenofibrate |
TABLET, FILM COATED |
ORAL |
20150307 |
N/A |
ANDA |
ANDA076635 |
Aphena Pharma Solutions - Tennessee, LLC |
FENOFIBRATE |
160 mg/1 |
3060 TABLET, FILM COATED in 1 BOTTLE (43353-001-19) |
63187-760-30 |
63187-760 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate |
Fenofibrate |
TABLET, FILM COATED |
ORAL |
20161101 |
N/A |
ANDA |
ANDA076635 |
Proficient Rx LP |
FENOFIBRATE |
160 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (63187-760-30) |
63187-760-60 |
63187-760 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate |
Fenofibrate |
TABLET, FILM COATED |
ORAL |
20161101 |
N/A |
ANDA |
ANDA076635 |
Proficient Rx LP |
FENOFIBRATE |
160 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (63187-760-60) |
63187-760-90 |
63187-760 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate |
Fenofibrate |
TABLET, FILM COATED |
ORAL |
20161101 |
N/A |
ANDA |
ANDA076635 |
Proficient Rx LP |
FENOFIBRATE |
160 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (63187-760-90) |
63304-901-03 |
63304-901 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate |
Fenofibrate |
TABLET, FILM COATED |
ORAL |
20200918 |
N/A |
ANDA |
ANDA076635 |
Sun Pharmaceutical Industries, Inc. |
FENOFIBRATE |
160 mg/1 |
10 TABLET, FILM COATED in 1 BOTTLE (63304-901-03) |
63304-901-10 |
63304-901 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate |
Fenofibrate |
TABLET, FILM COATED |
ORAL |
20200918 |
N/A |
ANDA |
ANDA076635 |
Sun Pharmaceutical Industries, Inc. |
FENOFIBRATE |
160 mg/1 |
1000 TABLET, FILM COATED in 1 BOTTLE (63304-901-10) |
63304-901-90 |
63304-901 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate |
Fenofibrate |
TABLET, FILM COATED |
ORAL |
20200918 |
N/A |
ANDA |
ANDA076635 |
Sun Pharmaceutical Industries, Inc. |
FENOFIBRATE |
160 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (63304-901-90) |
63629-2505-1 |
63629-2505 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate |
Fenofibrate |
TABLET, FILM COATED |
ORAL |
20210309 |
N/A |
ANDA |
ANDA076635 |
Bryant Ranch Prepack |
FENOFIBRATE |
160 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (63629-2505-1) |
63629-1099-1 |
63629-1099 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate |
Fenofibrate |
TABLET, FILM COATED |
ORAL |
20201118 |
N/A |
ANDA |
ANDA076635 |
Bryant Ranch Prepack |
FENOFIBRATE |
160 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (63629-1099-1) |
63629-1099-2 |
63629-1099 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate |
Fenofibrate |
TABLET, FILM COATED |
ORAL |
20210525 |
N/A |
ANDA |
ANDA076635 |
Bryant Ranch Prepack |
FENOFIBRATE |
160 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (63629-1099-2) |
63629-1099-3 |
63629-1099 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate |
Fenofibrate |
TABLET, FILM COATED |
ORAL |
20201102 |
N/A |
ANDA |
ANDA076635 |
Bryant Ranch Prepack |
FENOFIBRATE |
160 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (63629-1099-3) |
63629-1099-4 |
63629-1099 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate |
Fenofibrate |
TABLET, FILM COATED |
ORAL |
20210517 |
N/A |
ANDA |
ANDA076635 |
Bryant Ranch Prepack |
FENOFIBRATE |
160 mg/1 |
50 TABLET, FILM COATED in 1 BOTTLE (63629-1099-4) |
63629-1101-1 |
63629-1101 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate |
Fenofibrate |
TABLET, FILM COATED |
ORAL |
20200918 |
N/A |
ANDA |
ANDA076635 |
Bryant Ranch Prepack |
FENOFIBRATE |
54 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (63629-1101-1) |
63304-900-03 |
63304-900 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate |
Fenofibrate |
TABLET, FILM COATED |
ORAL |
20200918 |
N/A |
ANDA |
ANDA076635 |
Sun Pharmaceutical Industries, Inc. |
FENOFIBRATE |
54 mg/1 |
10 TABLET, FILM COATED in 1 BOTTLE (63304-900-03) |
63304-900-10 |
63304-900 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate |
Fenofibrate |
TABLET, FILM COATED |
ORAL |
20200918 |
N/A |
ANDA |
ANDA076635 |
Sun Pharmaceutical Industries, Inc. |
FENOFIBRATE |
54 mg/1 |
1000 TABLET, FILM COATED in 1 BOTTLE (63304-900-10) |
63304-900-90 |
63304-900 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate |
Fenofibrate |
TABLET, FILM COATED |
ORAL |
20200918 |
N/A |
ANDA |
ANDA076635 |
Sun Pharmaceutical Industries, Inc. |
FENOFIBRATE |
54 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (63304-900-90) |
63187-640-30 |
63187-640 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate |
Fenofibrate |
TABLET, FILM COATED |
ORAL |
20160201 |
N/A |
ANDA |
ANDA076635 |
Proficient Rx LP |
FENOFIBRATE |
54 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (63187-640-30) |
63187-640-60 |
63187-640 |
HUMAN PRESCRIPTION DRUG |
Fenofibrate |
Fenofibrate |
TABLET, FILM COATED |
ORAL |
20160201 |
N/A |
ANDA |
ANDA076635 |
Proficient Rx LP |
FENOFIBRATE |
54 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (63187-640-60) |