68382-531-01 |
68382-531 |
HUMAN PRESCRIPTION DRUG |
minocycline hydrochloride |
minocycline hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20180307 |
N/A |
ANDA |
ANDA203553 |
Zydus Pharmaceuticals (USA) Inc. |
MINOCYCLINE HYDROCHLORIDE |
45 mg/1 |
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-531-01) |
68382-531-05 |
68382-531 |
HUMAN PRESCRIPTION DRUG |
minocycline hydrochloride |
minocycline hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20180307 |
N/A |
ANDA |
ANDA203553 |
Zydus Pharmaceuticals (USA) Inc. |
MINOCYCLINE HYDROCHLORIDE |
45 mg/1 |
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-531-05) |
68382-531-06 |
68382-531 |
HUMAN PRESCRIPTION DRUG |
minocycline hydrochloride |
minocycline hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20180307 |
N/A |
ANDA |
ANDA203553 |
Zydus Pharmaceuticals (USA) Inc. |
MINOCYCLINE HYDROCHLORIDE |
45 mg/1 |
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-531-06) |
68382-531-10 |
68382-531 |
HUMAN PRESCRIPTION DRUG |
minocycline hydrochloride |
minocycline hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20180307 |
N/A |
ANDA |
ANDA203553 |
Zydus Pharmaceuticals (USA) Inc. |
MINOCYCLINE HYDROCHLORIDE |
45 mg/1 |
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-531-10) |
68382-531-16 |
68382-531 |
HUMAN PRESCRIPTION DRUG |
minocycline hydrochloride |
minocycline hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20180307 |
N/A |
ANDA |
ANDA203553 |
Zydus Pharmaceuticals (USA) Inc. |
MINOCYCLINE HYDROCHLORIDE |
45 mg/1 |
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-531-16) |
68382-531-30 |
68382-531 |
HUMAN PRESCRIPTION DRUG |
minocycline hydrochloride |
minocycline hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20180307 |
N/A |
ANDA |
ANDA203553 |
Zydus Pharmaceuticals (USA) Inc. |
MINOCYCLINE HYDROCHLORIDE |
45 mg/1 |
10 BLISTER PACK in 1 CARTON (68382-531-30) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
70771-1156-7 |
70771-1156 |
HUMAN PRESCRIPTION DRUG |
minocycline hydrochloride |
minocycline hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20180307 |
N/A |
ANDA |
ANDA203553 |
Zydus Lifesciences Limited |
MINOCYCLINE HYDROCHLORIDE |
90 mg/1 |
10 BLISTER PACK in 1 CARTON (70771-1156-7) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
70771-1156-9 |
70771-1156 |
HUMAN PRESCRIPTION DRUG |
minocycline hydrochloride |
minocycline hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20180307 |
N/A |
ANDA |
ANDA203553 |
Zydus Lifesciences Limited |
MINOCYCLINE HYDROCHLORIDE |
90 mg/1 |
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1156-9) |
68382-533-01 |
68382-533 |
HUMAN PRESCRIPTION DRUG |
minocycline hydrochloride |
minocycline hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20180307 |
N/A |
ANDA |
ANDA203553 |
Zydus Pharmaceuticals (USA) Inc. |
MINOCYCLINE HYDROCHLORIDE |
90 mg/1 |
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-533-01) |
68382-533-05 |
68382-533 |
HUMAN PRESCRIPTION DRUG |
minocycline hydrochloride |
minocycline hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20180307 |
N/A |
ANDA |
ANDA203553 |
Zydus Pharmaceuticals (USA) Inc. |
MINOCYCLINE HYDROCHLORIDE |
90 mg/1 |
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-533-05) |
68382-533-06 |
68382-533 |
HUMAN PRESCRIPTION DRUG |
minocycline hydrochloride |
minocycline hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20180307 |
N/A |
ANDA |
ANDA203553 |
Zydus Pharmaceuticals (USA) Inc. |
MINOCYCLINE HYDROCHLORIDE |
90 mg/1 |
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-533-06) |
68382-533-10 |
68382-533 |
HUMAN PRESCRIPTION DRUG |
minocycline hydrochloride |
minocycline hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20180307 |
N/A |
ANDA |
ANDA203553 |
Zydus Pharmaceuticals (USA) Inc. |
MINOCYCLINE HYDROCHLORIDE |
90 mg/1 |
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-533-10) |
68382-533-16 |
68382-533 |
HUMAN PRESCRIPTION DRUG |
minocycline hydrochloride |
minocycline hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20180307 |
N/A |
ANDA |
ANDA203553 |
Zydus Pharmaceuticals (USA) Inc. |
MINOCYCLINE HYDROCHLORIDE |
90 mg/1 |
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-533-16) |
68382-533-30 |
68382-533 |
HUMAN PRESCRIPTION DRUG |
minocycline hydrochloride |
minocycline hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20180307 |
N/A |
ANDA |
ANDA203553 |
Zydus Pharmaceuticals (USA) Inc. |
MINOCYCLINE HYDROCHLORIDE |
90 mg/1 |
10 BLISTER PACK in 1 CARTON (68382-533-30) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
70771-1157-0 |
70771-1157 |
HUMAN PRESCRIPTION DRUG |
minocycline hydrochloride |
minocycline hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20180307 |
N/A |
ANDA |
ANDA203553 |
Zydus Lifesciences Limited |
MINOCYCLINE HYDROCHLORIDE |
105 mg/1 |
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1157-0) |
70771-1157-1 |
70771-1157 |
HUMAN PRESCRIPTION DRUG |
minocycline hydrochloride |
minocycline hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20180307 |
N/A |
ANDA |
ANDA203553 |
Zydus Lifesciences Limited |
MINOCYCLINE HYDROCHLORIDE |
105 mg/1 |
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1157-1) |
68382-535-01 |
68382-535 |
HUMAN PRESCRIPTION DRUG |
minocycline hydrochloride |
minocycline hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20180307 |
N/A |
ANDA |
ANDA203553 |
Zydus Pharmaceuticals (USA) Inc. |
MINOCYCLINE HYDROCHLORIDE |
135 mg/1 |
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-535-01) |
68382-535-05 |
68382-535 |
HUMAN PRESCRIPTION DRUG |
minocycline hydrochloride |
minocycline hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20180307 |
N/A |
ANDA |
ANDA203553 |
Zydus Pharmaceuticals (USA) Inc. |
MINOCYCLINE HYDROCHLORIDE |
135 mg/1 |
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-535-05) |
68382-535-06 |
68382-535 |
HUMAN PRESCRIPTION DRUG |
minocycline hydrochloride |
minocycline hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20180307 |
N/A |
ANDA |
ANDA203553 |
Zydus Pharmaceuticals (USA) Inc. |
MINOCYCLINE HYDROCHLORIDE |
135 mg/1 |
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-535-06) |
68382-535-10 |
68382-535 |
HUMAN PRESCRIPTION DRUG |
minocycline hydrochloride |
minocycline hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20180307 |
N/A |
ANDA |
ANDA203553 |
Zydus Pharmaceuticals (USA) Inc. |
MINOCYCLINE HYDROCHLORIDE |
135 mg/1 |
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-535-10) |