68382-255-06 |
68382-255 |
HUMAN PRESCRIPTION DRUG |
oxybutynin |
oxybutynin |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20170810 |
N/A |
ANDA |
ANDA202332 |
Zydus Pharmaceuticals USA Inc. |
OXYBUTYNIN CHLORIDE |
5 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-255-06) |
68382-255-14 |
68382-255 |
HUMAN PRESCRIPTION DRUG |
oxybutynin |
oxybutynin |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20170810 |
N/A |
ANDA |
ANDA202332 |
Zydus Pharmaceuticals USA Inc. |
OXYBUTYNIN CHLORIDE |
5 mg/1 |
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-255-14) |
68382-255-16 |
68382-255 |
HUMAN PRESCRIPTION DRUG |
oxybutynin |
oxybutynin |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20170810 |
N/A |
ANDA |
ANDA202332 |
Zydus Pharmaceuticals USA Inc. |
OXYBUTYNIN CHLORIDE |
5 mg/1 |
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-255-16) |
68382-255-77 |
68382-255 |
HUMAN PRESCRIPTION DRUG |
oxybutynin |
oxybutynin |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20170810 |
N/A |
ANDA |
ANDA202332 |
Zydus Pharmaceuticals USA Inc. |
OXYBUTYNIN CHLORIDE |
5 mg/1 |
10 BLISTER PACK in 1 CARTON (68382-255-77) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68382-255-30) |
68382-255-05 |
68382-255 |
HUMAN PRESCRIPTION DRUG |
oxybutynin |
oxybutynin |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20170810 |
N/A |
ANDA |
ANDA202332 |
Zydus Pharmaceuticals USA Inc. |
OXYBUTYNIN CHLORIDE |
5 mg/1 |
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-255-05) |
68382-255-01 |
68382-255 |
HUMAN PRESCRIPTION DRUG |
oxybutynin |
oxybutynin |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20170810 |
N/A |
ANDA |
ANDA202332 |
Zydus Pharmaceuticals USA Inc. |
OXYBUTYNIN CHLORIDE |
5 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-255-01) |
50090-5353-0 |
50090-5353 |
HUMAN PRESCRIPTION DRUG |
oxybutynin |
oxybutynin |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20201111 |
N/A |
ANDA |
ANDA202332 |
A-S Medication Solutions |
OXYBUTYNIN CHLORIDE |
10 mg/1 |
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5353-0) |
68382-256-01 |
68382-256 |
HUMAN PRESCRIPTION DRUG |
oxybutynin |
oxybutynin |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20170810 |
N/A |
ANDA |
ANDA202332 |
Zydus Pharmaceuticals USA Inc. |
OXYBUTYNIN CHLORIDE |
10 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-256-01) |
68382-256-16 |
68382-256 |
HUMAN PRESCRIPTION DRUG |
oxybutynin |
oxybutynin |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20170810 |
N/A |
ANDA |
ANDA202332 |
Zydus Pharmaceuticals USA Inc. |
OXYBUTYNIN CHLORIDE |
10 mg/1 |
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-256-16) |
68382-256-77 |
68382-256 |
HUMAN PRESCRIPTION DRUG |
oxybutynin |
oxybutynin |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20170810 |
N/A |
ANDA |
ANDA202332 |
Zydus Pharmaceuticals USA Inc. |
OXYBUTYNIN CHLORIDE |
10 mg/1 |
10 BLISTER PACK in 1 CARTON (68382-256-77) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68382-256-30) |
68382-257-01 |
68382-257 |
HUMAN PRESCRIPTION DRUG |
oxybutynin |
oxybutynin |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20170810 |
N/A |
ANDA |
ANDA202332 |
Zydus Pharmaceuticals USA Inc. |
OXYBUTYNIN CHLORIDE |
15 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-257-01) |
68382-257-05 |
68382-257 |
HUMAN PRESCRIPTION DRUG |
oxybutynin |
oxybutynin |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20170810 |
N/A |
ANDA |
ANDA202332 |
Zydus Pharmaceuticals USA Inc. |
OXYBUTYNIN CHLORIDE |
15 mg/1 |
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-257-05) |
68382-257-06 |
68382-257 |
HUMAN PRESCRIPTION DRUG |
oxybutynin |
oxybutynin |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20170810 |
N/A |
ANDA |
ANDA202332 |
Zydus Pharmaceuticals USA Inc. |
OXYBUTYNIN CHLORIDE |
15 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-257-06) |
68382-257-14 |
68382-257 |
HUMAN PRESCRIPTION DRUG |
oxybutynin |
oxybutynin |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20170810 |
N/A |
ANDA |
ANDA202332 |
Zydus Pharmaceuticals USA Inc. |
OXYBUTYNIN CHLORIDE |
15 mg/1 |
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-257-14) |
68382-257-16 |
68382-257 |
HUMAN PRESCRIPTION DRUG |
oxybutynin |
oxybutynin |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20170810 |
N/A |
ANDA |
ANDA202332 |
Zydus Pharmaceuticals USA Inc. |
OXYBUTYNIN CHLORIDE |
15 mg/1 |
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-257-16) |
68382-257-77 |
68382-257 |
HUMAN PRESCRIPTION DRUG |
oxybutynin |
oxybutynin |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20170810 |
N/A |
ANDA |
ANDA202332 |
Zydus Pharmaceuticals USA Inc. |
OXYBUTYNIN CHLORIDE |
15 mg/1 |
10 BLISTER PACK in 1 CARTON (68382-257-77) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68382-257-30) |
68382-256-05 |
68382-256 |
HUMAN PRESCRIPTION DRUG |
oxybutynin |
oxybutynin |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20170810 |
N/A |
ANDA |
ANDA202332 |
Zydus Pharmaceuticals USA Inc. |
OXYBUTYNIN CHLORIDE |
10 mg/1 |
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-256-05) |
68382-256-06 |
68382-256 |
HUMAN PRESCRIPTION DRUG |
oxybutynin |
oxybutynin |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20170810 |
N/A |
ANDA |
ANDA202332 |
Zydus Pharmaceuticals USA Inc. |
OXYBUTYNIN CHLORIDE |
10 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-256-06) |
68382-256-14 |
68382-256 |
HUMAN PRESCRIPTION DRUG |
oxybutynin |
oxybutynin |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20170810 |
N/A |
ANDA |
ANDA202332 |
Zydus Pharmaceuticals USA Inc. |
OXYBUTYNIN CHLORIDE |
10 mg/1 |
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-256-14) |
0615-8219-39 |
0615-8219 |
HUMAN PRESCRIPTION DRUG |
oxybutynin |
oxybutynin |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20190125 |
N/A |
ANDA |
ANDA202332 |
NCS HealthCare of KY, LLC dba Vangard Labs |
OXYBUTYNIN CHLORIDE |
5 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-8219-39) |