82009-045-05 |
82009-045 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine sulfate |
Hydroxychloroquine sulfate |
TABLET, FILM COATED |
ORAL |
20220930 |
N/A |
ANDA |
ANDA040657 |
Quallent Pharmaceuticals Health LLC |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
500 TABLET, FILM COATED in 1 BOTTLE (82009-045-05) |
71335-0897-4 |
71335-0897 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine sulfate |
Hydroxychloroquine sulfate |
TABLET, FILM COATED |
ORAL |
20180710 |
N/A |
ANDA |
ANDA040657 |
Bryant Ranch Prepack |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
180 TABLET, FILM COATED in 1 BOTTLE (71335-0897-4) |
71335-0897-5 |
71335-0897 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine sulfate |
Hydroxychloroquine sulfate |
TABLET, FILM COATED |
ORAL |
20190225 |
N/A |
ANDA |
ANDA040657 |
Bryant Ranch Prepack |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (71335-0897-5) |
71335-0897-6 |
71335-0897 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine sulfate |
Hydroxychloroquine sulfate |
TABLET, FILM COATED |
ORAL |
20211227 |
N/A |
ANDA |
ANDA040657 |
Bryant Ranch Prepack |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
120 TABLET, FILM COATED in 1 BOTTLE (71335-0897-6) |
71335-0897-7 |
71335-0897 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine sulfate |
Hydroxychloroquine sulfate |
TABLET, FILM COATED |
ORAL |
20201223 |
N/A |
ANDA |
ANDA040657 |
Bryant Ranch Prepack |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
10 TABLET, FILM COATED in 1 BOTTLE (71335-0897-7) |
71335-0897-8 |
71335-0897 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine sulfate |
Hydroxychloroquine sulfate |
TABLET, FILM COATED |
ORAL |
20210118 |
N/A |
ANDA |
ANDA040657 |
Bryant Ranch Prepack |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
14 TABLET, FILM COATED in 1 BOTTLE (71335-0897-8) |
71335-0897-9 |
71335-0897 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine sulfate |
Hydroxychloroquine sulfate |
TABLET, FILM COATED |
ORAL |
20211227 |
N/A |
ANDA |
ANDA040657 |
Bryant Ranch Prepack |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
20 TABLET, FILM COATED in 1 BOTTLE (71335-0897-9) |
0615-8459-39 |
0615-8459 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine sulfate |
Hydroxychloroquine sulfate |
TABLET, FILM COATED |
ORAL |
20230413 |
N/A |
ANDA |
ANDA040657 |
NCS HealthCare of KY, LLC dba Vangard Labs |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8459-39) |
68071-2912-2 |
68071-2912 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine sulfate |
Hydroxychloroquine sulfate |
TABLET, FILM COATED |
ORAL |
20230125 |
N/A |
ANDA |
ANDA040657 |
NuCare Pharmaceuticals,Inc. |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
12 TABLET, FILM COATED in 1 BOTTLE (68071-2912-2) |
68071-2912-3 |
68071-2912 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine sulfate |
Hydroxychloroquine sulfate |
TABLET, FILM COATED |
ORAL |
20230125 |
N/A |
ANDA |
ANDA040657 |
NuCare Pharmaceuticals,Inc. |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (68071-2912-3) |
68071-2912-9 |
68071-2912 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine sulfate |
Hydroxychloroquine sulfate |
TABLET, FILM COATED |
ORAL |
20230111 |
N/A |
ANDA |
ANDA040657 |
NuCare Pharmaceuticals,Inc. |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (68071-2912-9) |
71610-506-30 |
71610-506 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine sulfate |
Hydroxychloroquine sulfate |
TABLET, FILM COATED |
ORAL |
20201222 |
N/A |
ANDA |
ANDA040657 |
Aphena Pharma Solutions - Tennessee, LLC |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (71610-506-30) |
71610-506-53 |
71610-506 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine sulfate |
Hydroxychloroquine sulfate |
TABLET, FILM COATED |
ORAL |
20201222 |
N/A |
ANDA |
ANDA040657 |
Aphena Pharma Solutions - Tennessee, LLC |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (71610-506-53) |
71335-0897-3 |
71335-0897 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine sulfate |
Hydroxychloroquine sulfate |
TABLET, FILM COATED |
ORAL |
20180706 |
N/A |
ANDA |
ANDA040657 |
Bryant Ranch Prepack |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (71335-0897-3) |
71335-0897-2 |
71335-0897 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine sulfate |
Hydroxychloroquine sulfate |
TABLET, FILM COATED |
ORAL |
20200313 |
N/A |
ANDA |
ANDA040657 |
Bryant Ranch Prepack |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (71335-0897-2) |
68382-096-77 |
68382-096 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine sulfate |
Hydroxychloroquine sulfate |
TABLET, FILM COATED |
ORAL |
20080103 |
N/A |
ANDA |
ANDA040657 |
Zydus Pharmaceuticals USA Inc. |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
100 BLISTER PACK in 1 CARTON (68382-096-77) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68382-096-30) |
68382-096-01 |
68382-096 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine sulfate |
Hydroxychloroquine sulfate |
TABLET, FILM COATED |
ORAL |
20080103 |
N/A |
ANDA |
ANDA040657 |
Zydus Pharmaceuticals USA Inc. |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (68382-096-01) |
68382-096-05 |
68382-096 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine sulfate |
Hydroxychloroquine sulfate |
TABLET, FILM COATED |
ORAL |
20080103 |
N/A |
ANDA |
ANDA040657 |
Zydus Pharmaceuticals USA Inc. |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
500 TABLET, FILM COATED in 1 BOTTLE (68382-096-05) |
68788-7747-2 |
68788-7747 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine sulfate |
Hydroxychloroquine sulfate |
TABLET, FILM COATED |
ORAL |
20200701 |
N/A |
ANDA |
ANDA040657 |
Preferred Pharmaceuticals, Inc. |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
20 TABLET, FILM COATED in 1 BOTTLE (68788-7747-2) |
68788-7747-3 |
68788-7747 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine sulfate |
Hydroxychloroquine sulfate |
TABLET, FILM COATED |
ORAL |
20200701 |
N/A |
ANDA |
ANDA040657 |
Preferred Pharmaceuticals, Inc. |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (68788-7747-3) |