16714-631-01 |
16714-631 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20080804 |
N/A |
ANDA |
ANDA090124 |
NorthStar Rx LLC |
ALENDRONATE SODIUM |
10 mg/1 |
30 TABLET in 1 BOTTLE (16714-631-01) |
16714-631-02 |
16714-631 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20080804 |
N/A |
ANDA |
ANDA090124 |
NorthStar Rx LLC |
ALENDRONATE SODIUM |
10 mg/1 |
100 TABLET in 1 BOTTLE (16714-631-02) |
16714-631-11 |
16714-631 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20080804 |
N/A |
ANDA |
ANDA090124 |
NorthStar Rx LLC |
ALENDRONATE SODIUM |
10 mg/1 |
10 BLISTER PACK in 1 CARTON (16714-631-11) / 10 TABLET in 1 BLISTER PACK (16714-631-10) |
50090-5677-0 |
50090-5677 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20210921 |
N/A |
ANDA |
ANDA090124 |
A-S Medication Solutions |
ALENDRONATE SODIUM |
70 mg/1 |
1 BLISTER PACK in 1 CARTON (50090-5677-0) / 4 TABLET in 1 BLISTER PACK |
50090-5677-1 |
50090-5677 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20210921 |
N/A |
ANDA |
ANDA090124 |
A-S Medication Solutions |
ALENDRONATE SODIUM |
70 mg/1 |
3 BLISTER PACK in 1 CARTON (50090-5677-1) / 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) |
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) |
65862-327-10 |
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 |
16714-633-01 |
16714-633 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20080804 |
N/A |
ANDA |
ANDA090124 |
NorthStar Rx LLC |
ALENDRONATE SODIUM |
70 mg/1 |
1 BLISTER PACK in 1 CARTON (16714-633-01) / 4 TABLET in 1 BLISTER PACK |
16714-633-02 |
16714-633 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20080804 |
N/A |
ANDA |
ANDA090124 |
NorthStar Rx LLC |
ALENDRONATE SODIUM |
70 mg/1 |
5 BLISTER PACK in 1 CARTON (16714-633-02) / 4 TABLET in 1 BLISTER PACK |
16714-633-11 |
16714-633 |
HUMAN PRESCRIPTION DRUG |
Alendronate Sodium |
Alendronate Sodium |
TABLET |
ORAL |
20080804 |
N/A |
ANDA |
ANDA090124 |
NorthStar Rx LLC |
ALENDRONATE SODIUM |
70 mg/1 |
10 BLISTER PACK in 1 CARTON (16714-633-11) / 10 TABLET in 1 BLISTER PACK (16714-633-10) |
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) |
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 |
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 |