| 57237-114-01 |
57237-114 |
HUMAN PRESCRIPTION DRUG |
Alfuzosin Hydrochloride |
Alfuzosin Hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20120830 |
N/A |
ANDA |
ANDA079060 |
Rising Pharma Holdings, Inc. |
ALFUZOSIN HYDROCHLORIDE |
10 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (57237-114-01) |
| 57237-114-05 |
57237-114 |
HUMAN PRESCRIPTION DRUG |
Alfuzosin Hydrochloride |
Alfuzosin Hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20120830 |
N/A |
ANDA |
ANDA079060 |
Rising Pharma Holdings, Inc. |
ALFUZOSIN HYDROCHLORIDE |
10 mg/1 |
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (57237-114-05) |
| 57237-114-90 |
57237-114 |
HUMAN PRESCRIPTION DRUG |
Alfuzosin Hydrochloride |
Alfuzosin Hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20120830 |
N/A |
ANDA |
ANDA079060 |
Rising Pharma Holdings, Inc. |
ALFUZOSIN HYDROCHLORIDE |
10 mg/1 |
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (57237-114-90) |
| 51655-087-52 |
51655-087 |
HUMAN PRESCRIPTION DRUG |
Alfuzosin Hydrochloride |
Alfuzosin Hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20221004 |
N/A |
ANDA |
ANDA079060 |
Northwind Pharmaceuticals, LLC |
ALFUZOSIN HYDROCHLORIDE |
10 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-087-52) |
| 71335-2578-1 |
71335-2578 |
HUMAN PRESCRIPTION DRUG |
Alfuzosin Hydrochloride |
Alfuzosin Hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20250206 |
N/A |
ANDA |
ANDA079060 |
Bryant Ranch Prepack |
ALFUZOSIN HYDROCHLORIDE |
10 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-1) |
| 71335-2578-2 |
71335-2578 |
HUMAN PRESCRIPTION DRUG |
Alfuzosin Hydrochloride |
Alfuzosin Hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20250206 |
N/A |
ANDA |
ANDA079060 |
Bryant Ranch Prepack |
ALFUZOSIN HYDROCHLORIDE |
10 mg/1 |
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-2) |
| 71335-2578-3 |
71335-2578 |
HUMAN PRESCRIPTION DRUG |
Alfuzosin Hydrochloride |
Alfuzosin Hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20250206 |
N/A |
ANDA |
ANDA079060 |
Bryant Ranch Prepack |
ALFUZOSIN HYDROCHLORIDE |
10 mg/1 |
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-3) |
| 71335-2578-4 |
71335-2578 |
HUMAN PRESCRIPTION DRUG |
Alfuzosin Hydrochloride |
Alfuzosin Hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20250206 |
N/A |
ANDA |
ANDA079060 |
Bryant Ranch Prepack |
ALFUZOSIN HYDROCHLORIDE |
10 mg/1 |
120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-4) |
| 71335-2578-5 |
71335-2578 |
HUMAN PRESCRIPTION DRUG |
Alfuzosin Hydrochloride |
Alfuzosin Hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20250206 |
N/A |
ANDA |
ANDA079060 |
Bryant Ranch Prepack |
ALFUZOSIN HYDROCHLORIDE |
10 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-5) |
| 65862-249-01 |
65862-249 |
HUMAN PRESCRIPTION DRUG |
Alfuzosin Hydrochloride |
Alfuzosin Hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20120830 |
N/A |
ANDA |
ANDA079060 |
Aurobindo Pharma Limited |
ALFUZOSIN HYDROCHLORIDE |
10 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-01) |
| 65862-249-05 |
65862-249 |
HUMAN PRESCRIPTION DRUG |
Alfuzosin Hydrochloride |
Alfuzosin Hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20120830 |
N/A |
ANDA |
ANDA079060 |
Aurobindo Pharma Limited |
ALFUZOSIN HYDROCHLORIDE |
10 mg/1 |
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-05) |
| 65862-249-30 |
65862-249 |
HUMAN PRESCRIPTION DRUG |
Alfuzosin Hydrochloride |
Alfuzosin Hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20120830 |
N/A |
ANDA |
ANDA079060 |
Aurobindo Pharma Limited |
ALFUZOSIN HYDROCHLORIDE |
10 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-30) |
| 65862-249-90 |
65862-249 |
HUMAN PRESCRIPTION DRUG |
Alfuzosin Hydrochloride |
Alfuzosin Hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20120830 |
N/A |
ANDA |
ANDA079060 |
Aurobindo Pharma Limited |
ALFUZOSIN HYDROCHLORIDE |
10 mg/1 |
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-90) |
| 65862-249-99 |
65862-249 |
HUMAN PRESCRIPTION DRUG |
Alfuzosin Hydrochloride |
Alfuzosin Hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20120830 |
N/A |
ANDA |
ANDA079060 |
Aurobindo Pharma Limited |
ALFUZOSIN HYDROCHLORIDE |
10 mg/1 |
1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-99) |