16571-112-01 |
16571-112 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine Sulfate |
Hydroxychloroquine Sulfate |
TABLET, FILM COATED |
ORAL |
20230529 |
N/A |
ANDA |
ANDA210959 |
Rising Pharma Holdings, Inc. |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (16571-112-01) |
16571-112-06 |
16571-112 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine Sulfate |
Hydroxychloroquine Sulfate |
TABLET, FILM COATED |
ORAL |
20230529 |
N/A |
ANDA |
ANDA210959 |
Rising Pharma Holdings, Inc. |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (16571-112-06) |
16571-112-10 |
16571-112 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine Sulfate |
Hydroxychloroquine Sulfate |
TABLET, FILM COATED |
ORAL |
20230529 |
N/A |
ANDA |
ANDA210959 |
Rising Pharma Holdings, Inc. |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
1000 TABLET, FILM COATED in 1 BOTTLE (16571-112-10) |
16571-112-50 |
16571-112 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine Sulfate |
Hydroxychloroquine Sulfate |
TABLET, FILM COATED |
ORAL |
20230529 |
N/A |
ANDA |
ANDA210959 |
Rising Pharma Holdings, Inc. |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
500 TABLET, FILM COATED in 1 BOTTLE (16571-112-50) |
16571-687-01 |
16571-687 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine Sulfate |
Hydroxychloroquine Sulfate |
TABLET, FILM COATED |
ORAL |
20190905 |
20250228 |
ANDA |
ANDA210959 |
Rising Pharma Holdings, Inc. |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (16571-687-01) |
16571-687-50 |
16571-687 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine Sulfate |
Hydroxychloroquine Sulfate |
TABLET, FILM COATED |
ORAL |
20190905 |
20250228 |
ANDA |
ANDA210959 |
Rising Pharma Holdings, Inc. |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
500 TABLET, FILM COATED in 1 BOTTLE (16571-687-50) |
42385-927-01 |
42385-927 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine Sulfate |
Hydroxychloroquine Sulfate |
TABLET, FILM COATED |
ORAL |
20190905 |
20250228 |
ANDA |
ANDA210959 |
Laurus Labs Limited |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (42385-927-01) |
42385-927-05 |
42385-927 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine Sulfate |
Hydroxychloroquine Sulfate |
TABLET, FILM COATED |
ORAL |
20190905 |
20250228 |
ANDA |
ANDA210959 |
Laurus Labs Limited |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
500 TABLET, FILM COATED in 1 BOTTLE (42385-927-05) |
42385-971-01 |
42385-971 |
HUMAN PRESCRIPTION DRUG |
HYDROXYCHLOROQUINE SULFATE |
HYDROXYCHLOROQUINE SULFATE |
TABLET, FILM COATED |
ORAL |
20230306 |
N/A |
ANDA |
ANDA210959 |
Laurus Labs Limited |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (42385-971-01) |
42385-971-05 |
42385-971 |
HUMAN PRESCRIPTION DRUG |
HYDROXYCHLOROQUINE SULFATE |
HYDROXYCHLOROQUINE SULFATE |
TABLET, FILM COATED |
ORAL |
20230306 |
N/A |
ANDA |
ANDA210959 |
Laurus Labs Limited |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
500 TABLET, FILM COATED in 1 BOTTLE (42385-971-05) |
42385-971-11 |
42385-971 |
HUMAN PRESCRIPTION DRUG |
HYDROXYCHLOROQUINE SULFATE |
HYDROXYCHLOROQUINE SULFATE |
TABLET, FILM COATED |
ORAL |
20230306 |
N/A |
ANDA |
ANDA210959 |
Laurus Labs Limited |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
1000 TABLET, FILM COATED in 1 BOTTLE (42385-971-11) |
42385-971-60 |
42385-971 |
HUMAN PRESCRIPTION DRUG |
HYDROXYCHLOROQUINE SULFATE |
HYDROXYCHLOROQUINE SULFATE |
TABLET, FILM COATED |
ORAL |
20230306 |
N/A |
ANDA |
ANDA210959 |
Laurus Labs Limited |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (42385-971-60) |
76420-643-01 |
76420-643 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine Sulfate |
Hydroxychloroquine Sulfate |
TABLET, FILM COATED |
ORAL |
20231031 |
N/A |
ANDA |
ANDA210959 |
Asclemed USA, Inc. |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (76420-643-01) |
76420-643-30 |
76420-643 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine Sulfate |
Hydroxychloroquine Sulfate |
TABLET, FILM COATED |
ORAL |
20231031 |
N/A |
ANDA |
ANDA210959 |
Asclemed USA, Inc. |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (76420-643-30) |
76420-643-60 |
76420-643 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine Sulfate |
Hydroxychloroquine Sulfate |
TABLET, FILM COATED |
ORAL |
20231031 |
N/A |
ANDA |
ANDA210959 |
Asclemed USA, Inc. |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (76420-643-60) |
76420-643-90 |
76420-643 |
HUMAN PRESCRIPTION DRUG |
Hydroxychloroquine Sulfate |
Hydroxychloroquine Sulfate |
TABLET, FILM COATED |
ORAL |
20231031 |
N/A |
ANDA |
ANDA210959 |
Asclemed USA, Inc. |
HYDROXYCHLOROQUINE SULFATE |
200 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (76420-643-90) |