| 60760-780-30 |
60760-780 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240508 |
N/A |
ANDA |
ANDA213324 |
ST. MARY'S MEDICAL PARK PHARMACY |
CYCLOBENZAPRINE HYDROCHLORIDE |
7.5 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-780-30) |
| 60760-780-60 |
60760-780 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240508 |
N/A |
ANDA |
ANDA213324 |
ST. MARY'S MEDICAL PARK PHARMACY |
CYCLOBENZAPRINE HYDROCHLORIDE |
7.5 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-780-60) |
| 60760-780-90 |
60760-780 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240409 |
N/A |
ANDA |
ANDA213324 |
ST. MARY'S MEDICAL PARK PHARMACY |
CYCLOBENZAPRINE HYDROCHLORIDE |
7.5 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-780-90) |
| 60760-780-92 |
60760-780 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240416 |
N/A |
ANDA |
ANDA213324 |
ST. MARY'S MEDICAL PARK PHARMACY |
CYCLOBENZAPRINE HYDROCHLORIDE |
7.5 mg/1 |
120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-780-92) |
| 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) |
| 50090-5711-2 |
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 |
30 TABLET, FILM COATED in 1 BOTTLE (50090-5711-2) |
| 50090-5711-3 |
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 |
60 TABLET, FILM COATED in 1 BOTTLE (50090-5711-3) |
| 50090-5711-4 |
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 |
100 TABLET, FILM COATED in 1 BOTTLE (50090-5711-4) |
| 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) |
| 68788-8706-3 |
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 |
30 TABLET, FILM COATED in 1 BOTTLE (68788-8706-3) |
| 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) |
| 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) |
| 68788-8706-9 |
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) |
| 76420-840-20 |
76420-840 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240816 |
N/A |
ANDA |
ANDA213324 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
7.5 mg/1 |
20 TABLET, FILM COATED in 1 BOTTLE (76420-840-20) |
| 76420-840-30 |
76420-840 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240816 |
N/A |
ANDA |
ANDA213324 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
7.5 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (76420-840-30) |
| 76420-840-60 |
76420-840 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240816 |
N/A |
ANDA |
ANDA213324 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
7.5 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (76420-840-60) |
| 76420-840-90 |
76420-840 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine hydrochloride |
Cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240816 |
N/A |
ANDA |
ANDA213324 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
7.5 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (76420-840-90) |
| 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) |