| 68084-949-25 |
68084-949 |
HUMAN PRESCRIPTION DRUG |
Albuterol Sulfate |
Albuterol Sulfate |
TABLET |
ORAL |
20150818 |
N/A |
ANDA |
ANDA072637 |
American Health Packaging |
ALBUTEROL SULFATE |
2 mg/1 |
30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-949-25) / 1 TABLET in 1 BLISTER PACK (68084-949-95) |
| 68084-952-25 |
68084-952 |
HUMAN PRESCRIPTION DRUG |
albuterol sulfate |
albuterol sulfate |
TABLET |
ORAL |
20150916 |
N/A |
ANDA |
ANDA072637 |
American Health Packaging |
ALBUTEROL SULFATE |
4 mg/1 |
30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-952-25) / 1 TABLET in 1 BLISTER PACK (68084-952-95) |
| 51407-368-01 |
51407-368 |
HUMAN PRESCRIPTION DRUG |
albuterol sulfate |
albuterol sulfate |
TABLET |
ORAL |
20200326 |
N/A |
ANDA |
ANDA072637 |
Golden State Medical Supply |
ALBUTEROL SULFATE |
4 mg/1 |
100 TABLET in 1 BOTTLE (51407-368-01) |
| 51407-367-01 |
51407-367 |
HUMAN PRESCRIPTION DRUG |
albuterol sulfate |
albuterol sulfate |
TABLET |
ORAL |
20200326 |
N/A |
ANDA |
ANDA072637 |
Golden State Medical Supply |
ALBUTEROL SULFATE |
2 mg/1 |
100 TABLET in 1 BOTTLE (51407-367-01) |
| 53489-176-02 |
53489-176 |
HUMAN PRESCRIPTION DRUG |
albuterol sulfate |
albuterol sulfate |
TABLET |
ORAL |
19891205 |
N/A |
ANDA |
ANDA072637 |
Sun Pharmaceutical Industries, Inc. |
ALBUTEROL SULFATE |
2 mg/1 |
50 TABLET in 1 BOTTLE (53489-176-02) |
| 53489-176-10 |
53489-176 |
HUMAN PRESCRIPTION DRUG |
albuterol sulfate |
albuterol sulfate |
TABLET |
ORAL |
19891205 |
N/A |
ANDA |
ANDA072637 |
Sun Pharmaceutical Industries, Inc. |
ALBUTEROL SULFATE |
2 mg/1 |
1000 TABLET in 1 BOTTLE (53489-176-10) |
| 53489-177-01 |
53489-177 |
HUMAN PRESCRIPTION DRUG |
albuterol sulfate |
albuterol sulfate |
TABLET |
ORAL |
19891205 |
N/A |
ANDA |
ANDA072637 |
Sun Pharmaceutical Industries, Inc. |
ALBUTEROL SULFATE |
4 mg/1 |
100 TABLET in 1 BOTTLE (53489-177-01) |
| 53489-177-02 |
53489-177 |
HUMAN PRESCRIPTION DRUG |
albuterol sulfate |
albuterol sulfate |
TABLET |
ORAL |
19891205 |
N/A |
ANDA |
ANDA072637 |
Sun Pharmaceutical Industries, Inc. |
ALBUTEROL SULFATE |
4 mg/1 |
50 TABLET in 1 BOTTLE (53489-177-02) |
| 53489-177-03 |
53489-177 |
HUMAN PRESCRIPTION DRUG |
albuterol sulfate |
albuterol sulfate |
TABLET |
ORAL |
19891205 |
N/A |
ANDA |
ANDA072637 |
Sun Pharmaceutical Industries, Inc. |
ALBUTEROL SULFATE |
4 mg/1 |
250 TABLET in 1 BOTTLE (53489-177-03) |
| 53489-177-05 |
53489-177 |
HUMAN PRESCRIPTION DRUG |
albuterol sulfate |
albuterol sulfate |
TABLET |
ORAL |
19891205 |
N/A |
ANDA |
ANDA072637 |
Sun Pharmaceutical Industries, Inc. |
ALBUTEROL SULFATE |
4 mg/1 |
500 TABLET in 1 BOTTLE (53489-177-05) |
| 53489-177-10 |
53489-177 |
HUMAN PRESCRIPTION DRUG |
albuterol sulfate |
albuterol sulfate |
TABLET |
ORAL |
19891205 |
N/A |
ANDA |
ANDA072637 |
Sun Pharmaceutical Industries, Inc. |
ALBUTEROL SULFATE |
4 mg/1 |
1000 TABLET in 1 BOTTLE (53489-177-10) |
| 53489-176-01 |
53489-176 |
HUMAN PRESCRIPTION DRUG |
albuterol sulfate |
albuterol sulfate |
TABLET |
ORAL |
19891205 |
N/A |
ANDA |
ANDA072637 |
Sun Pharmaceutical Industries, Inc. |
ALBUTEROL SULFATE |
2 mg/1 |
100 TABLET in 1 BOTTLE (53489-176-01) |
| 53489-176-03 |
53489-176 |
HUMAN PRESCRIPTION DRUG |
albuterol sulfate |
albuterol sulfate |
TABLET |
ORAL |
19891205 |
N/A |
ANDA |
ANDA072637 |
Sun Pharmaceutical Industries, Inc. |
ALBUTEROL SULFATE |
2 mg/1 |
250 TABLET in 1 BOTTLE (53489-176-03) |
| 53489-176-05 |
53489-176 |
HUMAN PRESCRIPTION DRUG |
albuterol sulfate |
albuterol sulfate |
TABLET |
ORAL |
19891205 |
N/A |
ANDA |
ANDA072637 |
Sun Pharmaceutical Industries, Inc. |
ALBUTEROL SULFATE |
2 mg/1 |
500 TABLET in 1 BOTTLE (53489-176-05) |