| 65862-986-01 |
65862-986 |
HUMAN PRESCRIPTION DRUG |
Potassium Chloride |
Potassium Chloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20181219 |
N/A |
ANDA |
ANDA210921 |
Aurobindo Pharma Limited |
POTASSIUM CHLORIDE |
600 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-986-01) |
| 65862-986-05 |
65862-986 |
HUMAN PRESCRIPTION DRUG |
Potassium Chloride |
Potassium Chloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20181219 |
N/A |
ANDA |
ANDA210921 |
Aurobindo Pharma Limited |
POTASSIUM CHLORIDE |
600 mg/1 |
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-986-05) |
| 65862-986-12 |
65862-986 |
HUMAN PRESCRIPTION DRUG |
Potassium Chloride |
Potassium Chloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20181219 |
N/A |
ANDA |
ANDA210921 |
Aurobindo Pharma Limited |
POTASSIUM CHLORIDE |
600 mg/1 |
120 BLISTER PACK in 1 CARTON (65862-986-12) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-986-06) |
| 65862-986-80 |
65862-986 |
HUMAN PRESCRIPTION DRUG |
Potassium Chloride |
Potassium Chloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20181219 |
N/A |
ANDA |
ANDA210921 |
Aurobindo Pharma Limited |
POTASSIUM CHLORIDE |
600 mg/1 |
80 BLISTER PACK in 1 CARTON (65862-986-80) / 4 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-986-04) |
| 65862-987-01 |
65862-987 |
HUMAN PRESCRIPTION DRUG |
Potassium Chloride |
Potassium Chloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20181219 |
N/A |
ANDA |
ANDA210921 |
Aurobindo Pharma Limited |
POTASSIUM CHLORIDE |
750 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-987-01) |
| 65862-987-12 |
65862-987 |
HUMAN PRESCRIPTION DRUG |
Potassium Chloride |
Potassium Chloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20181219 |
N/A |
ANDA |
ANDA210921 |
Aurobindo Pharma Limited |
POTASSIUM CHLORIDE |
750 mg/1 |
120 BLISTER PACK in 1 CARTON (65862-987-12) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-987-06) |
| 65862-987-80 |
65862-987 |
HUMAN PRESCRIPTION DRUG |
Potassium Chloride |
Potassium Chloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20181219 |
N/A |
ANDA |
ANDA210921 |
Aurobindo Pharma Limited |
POTASSIUM CHLORIDE |
750 mg/1 |
80 BLISTER PACK in 1 CARTON (65862-987-80) / 4 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-987-04) |
| 65862-987-99 |
65862-987 |
HUMAN PRESCRIPTION DRUG |
Potassium Chloride |
Potassium Chloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20181219 |
N/A |
ANDA |
ANDA210921 |
Aurobindo Pharma Limited |
POTASSIUM CHLORIDE |
750 mg/1 |
1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-987-99) |
| 71610-944-30 |
71610-944 |
HUMAN PRESCRIPTION DRUG |
Potassium Chloride |
Potassium Chloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20250903 |
N/A |
ANDA |
ANDA210921 |
Aphena Pharma Solutions - Tennessee, LLC |
POTASSIUM CHLORIDE |
750 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-944-30) |
| 71610-944-53 |
71610-944 |
HUMAN PRESCRIPTION DRUG |
Potassium Chloride |
Potassium Chloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20250903 |
N/A |
ANDA |
ANDA210921 |
Aphena Pharma Solutions - Tennessee, LLC |
POTASSIUM CHLORIDE |
750 mg/1 |
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-944-53) |
| 71610-944-60 |
71610-944 |
HUMAN PRESCRIPTION DRUG |
Potassium Chloride |
Potassium Chloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20250903 |
N/A |
ANDA |
ANDA210921 |
Aphena Pharma Solutions - Tennessee, LLC |
POTASSIUM CHLORIDE |
750 mg/1 |
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-944-60) |
| 71610-944-70 |
71610-944 |
HUMAN PRESCRIPTION DRUG |
Potassium Chloride |
Potassium Chloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20250903 |
N/A |
ANDA |
ANDA210921 |
Aphena Pharma Solutions - Tennessee, LLC |
POTASSIUM CHLORIDE |
750 mg/1 |
120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-944-70) |
| 63629-2620-1 |
63629-2620 |
HUMAN PRESCRIPTION DRUG |
Potassium Chloride |
Potassium Chloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20240206 |
N/A |
ANDA |
ANDA210921 |
Bryant Ranch Prepack |
POTASSIUM CHLORIDE |
600 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-1) |
| 63629-2620-2 |
63629-2620 |
HUMAN PRESCRIPTION DRUG |
Potassium Chloride |
Potassium Chloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20240206 |
N/A |
ANDA |
ANDA210921 |
Bryant Ranch Prepack |
POTASSIUM CHLORIDE |
600 mg/1 |
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-2) |
| 63629-2620-3 |
63629-2620 |
HUMAN PRESCRIPTION DRUG |
Potassium Chloride |
Potassium Chloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20240206 |
N/A |
ANDA |
ANDA210921 |
Bryant Ranch Prepack |
POTASSIUM CHLORIDE |
600 mg/1 |
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-3) |
| 63629-2620-4 |
63629-2620 |
HUMAN PRESCRIPTION DRUG |
Potassium Chloride |
Potassium Chloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20240206 |
N/A |
ANDA |
ANDA210921 |
Bryant Ranch Prepack |
POTASSIUM CHLORIDE |
600 mg/1 |
180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-4) |
| 63629-2620-5 |
63629-2620 |
HUMAN PRESCRIPTION DRUG |
Potassium Chloride |
Potassium Chloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20240206 |
N/A |
ANDA |
ANDA210921 |
Bryant Ranch Prepack |
POTASSIUM CHLORIDE |
600 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-5) |
| 63629-2620-6 |
63629-2620 |
HUMAN PRESCRIPTION DRUG |
Potassium Chloride |
Potassium Chloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20240206 |
N/A |
ANDA |
ANDA210921 |
Bryant Ranch Prepack |
POTASSIUM CHLORIDE |
600 mg/1 |
20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-6) |
| 50090-5335-0 |
50090-5335 |
HUMAN PRESCRIPTION DRUG |
Potassium Chloride |
Potassium Chloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20201104 |
N/A |
ANDA |
ANDA210921 |
A-S Medication Solutions |
POTASSIUM CHLORIDE |
750 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5335-0) |
| 50090-5335-1 |
50090-5335 |
HUMAN PRESCRIPTION DRUG |
Potassium Chloride |
Potassium Chloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20201104 |
N/A |
ANDA |
ANDA210921 |
A-S Medication Solutions |
POTASSIUM CHLORIDE |
750 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5335-1) |