64896-695-01 |
64896-695 |
HUMAN PRESCRIPTION DRUG |
Oxymorphone hydrochloride |
Oxymorphone hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20130102 |
N/A |
ANDA |
ANDA079087 |
Amneal Pharmaceuticals LLC |
OXYMORPHONE HYDROCHLORIDE |
5 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-695-01) |
64896-695-03 |
64896-695 |
HUMAN PRESCRIPTION DRUG |
Oxymorphone hydrochloride |
Oxymorphone hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20130102 |
N/A |
ANDA |
ANDA079087 |
Amneal Pharmaceuticals LLC |
OXYMORPHONE HYDROCHLORIDE |
5 mg/1 |
1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-695-03) |
64896-695-08 |
64896-695 |
HUMAN PRESCRIPTION DRUG |
Oxymorphone hydrochloride |
Oxymorphone hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20130102 |
N/A |
ANDA |
ANDA079087 |
Amneal Pharmaceuticals LLC |
OXYMORPHONE HYDROCHLORIDE |
5 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-695-08) |
64896-695-13 |
64896-695 |
HUMAN PRESCRIPTION DRUG |
Oxymorphone hydrochloride |
Oxymorphone hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20130102 |
N/A |
ANDA |
ANDA079087 |
Amneal Pharmaceuticals LLC |
OXYMORPHONE HYDROCHLORIDE |
5 mg/1 |
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-695-13) |
64896-696-01 |
64896-696 |
HUMAN PRESCRIPTION DRUG |
Oxymorphone hydrochloride |
Oxymorphone hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20130102 |
N/A |
ANDA |
ANDA079087 |
Amneal Pharmaceuticals LLC |
OXYMORPHONE HYDROCHLORIDE |
7.5 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-696-01) |
64896-696-03 |
64896-696 |
HUMAN PRESCRIPTION DRUG |
Oxymorphone hydrochloride |
Oxymorphone hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20130102 |
N/A |
ANDA |
ANDA079087 |
Amneal Pharmaceuticals LLC |
OXYMORPHONE HYDROCHLORIDE |
7.5 mg/1 |
1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-696-03) |
64896-696-08 |
64896-696 |
HUMAN PRESCRIPTION DRUG |
Oxymorphone hydrochloride |
Oxymorphone hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20130102 |
N/A |
ANDA |
ANDA079087 |
Amneal Pharmaceuticals LLC |
OXYMORPHONE HYDROCHLORIDE |
7.5 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-696-08) |
64896-696-13 |
64896-696 |
HUMAN PRESCRIPTION DRUG |
Oxymorphone hydrochloride |
Oxymorphone hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20130102 |
N/A |
ANDA |
ANDA079087 |
Amneal Pharmaceuticals LLC |
OXYMORPHONE HYDROCHLORIDE |
7.5 mg/1 |
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-696-13) |
64896-697-01 |
64896-697 |
HUMAN PRESCRIPTION DRUG |
Oxymorphone hydrochloride |
Oxymorphone hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20130102 |
N/A |
ANDA |
ANDA079087 |
Amneal Pharmaceuticals LLC |
OXYMORPHONE HYDROCHLORIDE |
10 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-697-01) |
64896-697-03 |
64896-697 |
HUMAN PRESCRIPTION DRUG |
Oxymorphone hydrochloride |
Oxymorphone hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20130102 |
N/A |
ANDA |
ANDA079087 |
Amneal Pharmaceuticals LLC |
OXYMORPHONE HYDROCHLORIDE |
10 mg/1 |
1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-697-03) |
64896-697-08 |
64896-697 |
HUMAN PRESCRIPTION DRUG |
Oxymorphone hydrochloride |
Oxymorphone hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20130102 |
N/A |
ANDA |
ANDA079087 |
Amneal Pharmaceuticals LLC |
OXYMORPHONE HYDROCHLORIDE |
10 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-697-08) |
64896-697-13 |
64896-697 |
HUMAN PRESCRIPTION DRUG |
Oxymorphone hydrochloride |
Oxymorphone hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20130102 |
N/A |
ANDA |
ANDA079087 |
Amneal Pharmaceuticals LLC |
OXYMORPHONE HYDROCHLORIDE |
10 mg/1 |
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-697-13) |
64896-698-01 |
64896-698 |
HUMAN PRESCRIPTION DRUG |
Oxymorphone hydrochloride |
Oxymorphone hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20130102 |
N/A |
ANDA |
ANDA079087 |
Amneal Pharmaceuticals LLC |
OXYMORPHONE HYDROCHLORIDE |
15 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-698-01) |
64896-698-03 |
64896-698 |
HUMAN PRESCRIPTION DRUG |
Oxymorphone hydrochloride |
Oxymorphone hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20130102 |
N/A |
ANDA |
ANDA079087 |
Amneal Pharmaceuticals LLC |
OXYMORPHONE HYDROCHLORIDE |
15 mg/1 |
1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-698-03) |
64896-698-08 |
64896-698 |
HUMAN PRESCRIPTION DRUG |
Oxymorphone hydrochloride |
Oxymorphone hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20130102 |
N/A |
ANDA |
ANDA079087 |
Amneal Pharmaceuticals LLC |
OXYMORPHONE HYDROCHLORIDE |
15 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-698-08) |
64896-698-13 |
64896-698 |
HUMAN PRESCRIPTION DRUG |
Oxymorphone hydrochloride |
Oxymorphone hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20130102 |
N/A |
ANDA |
ANDA079087 |
Amneal Pharmaceuticals LLC |
OXYMORPHONE HYDROCHLORIDE |
15 mg/1 |
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-698-13) |
64896-699-01 |
64896-699 |
HUMAN PRESCRIPTION DRUG |
Oxymorphone hydrochloride |
Oxymorphone hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20130102 |
N/A |
ANDA |
ANDA079087 |
Amneal Pharmaceuticals LLC |
OXYMORPHONE HYDROCHLORIDE |
20 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-699-01) |
64896-699-03 |
64896-699 |
HUMAN PRESCRIPTION DRUG |
Oxymorphone hydrochloride |
Oxymorphone hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20130102 |
N/A |
ANDA |
ANDA079087 |
Amneal Pharmaceuticals LLC |
OXYMORPHONE HYDROCHLORIDE |
20 mg/1 |
1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-699-03) |
64896-699-08 |
64896-699 |
HUMAN PRESCRIPTION DRUG |
Oxymorphone hydrochloride |
Oxymorphone hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20130102 |
N/A |
ANDA |
ANDA079087 |
Amneal Pharmaceuticals LLC |
OXYMORPHONE HYDROCHLORIDE |
20 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-699-08) |
64896-699-13 |
64896-699 |
HUMAN PRESCRIPTION DRUG |
Oxymorphone hydrochloride |
Oxymorphone hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20130102 |
N/A |
ANDA |
ANDA079087 |
Amneal Pharmaceuticals LLC |
OXYMORPHONE HYDROCHLORIDE |
20 mg/1 |
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-699-13) |