| 65862-327-01 |
65862-327 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20080804 |
N/A |
ANDA |
ANDA090124 |
Aurobindo Pharma Limited |
ALENDRONATE SODIUM |
10 mg/1 |
100 TABLET in 1 BOTTLE (65862-327-01) |
| 65862-327-99 |
65862-327 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20080804 |
N/A |
ANDA |
ANDA090124 |
Aurobindo Pharma Limited |
ALENDRONATE SODIUM |
10 mg/1 |
1000 TABLET in 1 BOTTLE (65862-327-99) |
| 65862-327-10 |
65862-327 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20080804 |
N/A |
ANDA |
ANDA090124 |
Aurobindo Pharma Limited |
ALENDRONATE SODIUM |
10 mg/1 |
10 BLISTER PACK in 1 CARTON (65862-327-10) / 10 TABLET in 1 BLISTER PACK |
| 65862-328-10 |
65862-328 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20080804 |
N/A |
ANDA |
ANDA090124 |
Aurobindo Pharma Limited |
ALENDRONATE SODIUM |
35 mg/1 |
10 BLISTER PACK in 1 CARTON (65862-328-10) / 10 TABLET in 1 BLISTER PACK |
| 65862-329-05 |
65862-329 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20240306 |
N/A |
ANDA |
ANDA090124 |
Aurobindo Pharma Limited |
ALENDRONATE SODIUM |
70 mg/1 |
500 TABLET in 1 BOTTLE (65862-329-05) |
| 65862-329-08 |
65862-329 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20080804 |
N/A |
ANDA |
ANDA090124 |
Aurobindo Pharma Limited |
ALENDRONATE SODIUM |
70 mg/1 |
3 BLISTER PACK in 1 CARTON (65862-329-08) / 4 TABLET in 1 BLISTER PACK |
| 65862-329-10 |
65862-329 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20080804 |
N/A |
ANDA |
ANDA090124 |
Aurobindo Pharma Limited |
ALENDRONATE SODIUM |
70 mg/1 |
10 BLISTER PACK in 1 CARTON (65862-329-10) / 10 TABLET in 1 BLISTER PACK |
| 65862-329-20 |
65862-329 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20080804 |
N/A |
ANDA |
ANDA090124 |
Aurobindo Pharma Limited |
ALENDRONATE SODIUM |
70 mg/1 |
5 BLISTER PACK in 1 CARTON (65862-329-20) / 4 TABLET in 1 BLISTER PACK |
| 65862-328-20 |
65862-328 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20080804 |
N/A |
ANDA |
ANDA090124 |
Aurobindo Pharma Limited |
ALENDRONATE SODIUM |
35 mg/1 |
5 BLISTER PACK in 1 CARTON (65862-328-20) / 4 TABLET in 1 BLISTER PACK |
| 65862-329-01 |
65862-329 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20240306 |
N/A |
ANDA |
ANDA090124 |
Aurobindo Pharma Limited |
ALENDRONATE SODIUM |
70 mg/1 |
100 TABLET in 1 BOTTLE (65862-329-01) |
| 65862-329-04 |
65862-329 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20080804 |
N/A |
ANDA |
ANDA090124 |
Aurobindo Pharma Limited |
ALENDRONATE SODIUM |
70 mg/1 |
1 BLISTER PACK in 1 CARTON (65862-329-04) / 4 TABLET in 1 BLISTER PACK |
| 71205-048-04 |
71205-048 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20180601 |
N/A |
ANDA |
ANDA090124 |
Proficient Rx LP |
ALENDRONATE SODIUM |
70 mg/1 |
1 BLISTER PACK in 1 CARTON (71205-048-04) / 4 TABLET in 1 BLISTER PACK |
| 64980-341-14 |
64980-341 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20080804 |
N/A |
ANDA |
ANDA090124 |
Rising Pharma Holdings, Inc. |
ALENDRONATE SODIUM |
35 mg/1 |
1 BLISTER PACK in 1 CARTON (64980-341-14) / 4 TABLET in 1 BLISTER PACK |
| 64980-342-01 |
64980-342 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20240930 |
N/A |
ANDA |
ANDA090124 |
Rising Pharma Holdings, Inc. |
ALENDRONATE SODIUM |
70 mg/1 |
100 TABLET in 1 BOTTLE (64980-342-01) |
| 64980-342-14 |
64980-342 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20080804 |
N/A |
ANDA |
ANDA090124 |
Rising Pharma Holdings, Inc. |
ALENDRONATE SODIUM |
70 mg/1 |
1 BLISTER PACK in 1 CARTON (64980-342-14) / 4 TABLET in 1 BLISTER PACK |
| 64980-342-50 |
64980-342 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20240930 |
N/A |
ANDA |
ANDA090124 |
Rising Pharma Holdings, Inc. |
ALENDRONATE SODIUM |
70 mg/1 |
500 TABLET in 1 BOTTLE (64980-342-50) |
| 64980-340-01 |
64980-340 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20080804 |
N/A |
ANDA |
ANDA090124 |
Rising Pharma Holdings, Inc. |
ALENDRONATE SODIUM |
10 mg/1 |
100 TABLET in 1 BOTTLE (64980-340-01) |
| 64980-340-03 |
64980-340 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20080804 |
N/A |
ANDA |
ANDA090124 |
Rising Pharma Holdings, Inc. |
ALENDRONATE SODIUM |
10 mg/1 |
30 TABLET in 1 BOTTLE (64980-340-03) |
| 64980-341-12 |
64980-341 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20080804 |
N/A |
ANDA |
ANDA090124 |
Rising Pharma Holdings, Inc. |
ALENDRONATE SODIUM |
35 mg/1 |
3 BLISTER PACK in 1 CARTON (64980-341-12) / 4 TABLET in 1 BLISTER PACK |