| 70518-4265-0 |
70518-4265 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20250124 |
N/A |
ANDA |
ANDA213324 |
REMEDYREPACK INC. |
CYCLOBENZAPRINE HYDROCHLORIDE |
7.5 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4265-0) |
| 68071-2471-1 |
68071-2471 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20210707 |
N/A |
ANDA |
ANDA213324 |
NuCare Pharmaceuticals,Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
7.5 mg/1 |
15 TABLET, FILM COATED in 1 BOTTLE (68071-2471-1) |
| 68071-2471-2 |
68071-2471 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20210707 |
N/A |
ANDA |
ANDA213324 |
NuCare Pharmaceuticals,Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
7.5 mg/1 |
20 TABLET, FILM COATED in 1 BOTTLE (68071-2471-2) |
| 68071-2471-7 |
68071-2471 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240311 |
N/A |
ANDA |
ANDA213324 |
NuCare Pharmaceuticals,Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
7.5 mg/1 |
21 TABLET, FILM COATED in 1 BOTTLE (68071-2471-7) |
| 68071-2471-9 |
68071-2471 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20210707 |
N/A |
ANDA |
ANDA213324 |
NuCare Pharmaceuticals,Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
7.5 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (68071-2471-9) |
| 68071-3404-3 |
68071-3404 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine Hydrochloride |
Cyclobenzaprine Hydrochloride |
TABLET, FILM COATED |
ORAL |
20230516 |
N/A |
ANDA |
ANDA213324 |
NuCare Pharmaceuticals,Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (68071-3404-3) |
| 68071-3567-2 |
68071-3567 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240202 |
N/A |
ANDA |
ANDA213324 |
NuCare Pharmaceuticals,Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
12 TABLET, FILM COATED in 1 BOTTLE (68071-3567-2) |
| 68071-3567-3 |
68071-3567 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240202 |
N/A |
ANDA |
ANDA213324 |
NuCare Pharmaceuticals,Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (68071-3567-3) |
| 67296-1441-1 |
67296-1441 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20200706 |
N/A |
ANDA |
ANDA213324 |
Redpharm Drug, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
10 TABLET, FILM COATED in 1 BOTTLE (67296-1441-1) |
| 68788-8637-2 |
68788-8637 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240419 |
N/A |
ANDA |
ANDA213324 |
Preferred Pharmaceuticals Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
20 TABLET, FILM COATED in 1 BOTTLE (68788-8637-2) |
| 68788-8637-3 |
68788-8637 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240419 |
N/A |
ANDA |
ANDA213324 |
Preferred Pharmaceuticals Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (68788-8637-3) |
| 68788-8637-5 |
68788-8637 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240419 |
N/A |
ANDA |
ANDA213324 |
Preferred Pharmaceuticals Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
15 TABLET, FILM COATED in 1 BOTTLE (68788-8637-5) |
| 68788-8637-6 |
68788-8637 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240419 |
N/A |
ANDA |
ANDA213324 |
Preferred Pharmaceuticals Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (68788-8637-6) |
| 68788-8637-9 |
68788-8637 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240419 |
N/A |
ANDA |
ANDA213324 |
Preferred Pharmaceuticals Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (68788-8637-9) |
| 68788-8706-2 |
68788-8706 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240701 |
N/A |
ANDA |
ANDA213324 |
Preferred Pharmaceuticals Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
20 TABLET, FILM COATED in 1 BOTTLE (68788-8706-2) |
| 68788-8706-9 |
68788-8706 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240701 |
N/A |
ANDA |
ANDA213324 |
Preferred Pharmaceuticals Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (68788-8706-9) |
| 68788-8706-8 |
68788-8706 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240701 |
N/A |
ANDA |
ANDA213324 |
Preferred Pharmaceuticals Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
120 TABLET, FILM COATED in 1 BOTTLE (68788-8706-8) |
| 68788-8706-6 |
68788-8706 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240701 |
N/A |
ANDA |
ANDA213324 |
Preferred Pharmaceuticals Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (68788-8706-6) |
| 50090-5711-0 |
50090-5711 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20210924 |
N/A |
ANDA |
ANDA213324 |
A-S Medication Solutions |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
15 TABLET, FILM COATED in 1 BOTTLE (50090-5711-0) |
| 50090-5711-1 |
50090-5711 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20210924 |
N/A |
ANDA |
ANDA213324 |
A-S Medication Solutions |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
20 TABLET, FILM COATED in 1 BOTTLE (50090-5711-1) |