| 70518-3415-6 |
70518-3415 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240924 |
N/A |
ANDA |
ANDA208170 |
REMEDYREPACK INC. |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3415-6) |
| 70518-3415-1 |
70518-3415 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240430 |
N/A |
ANDA |
ANDA208170 |
REMEDYREPACK INC. |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3415-1) |
| 70518-3415-5 |
70518-3415 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240918 |
N/A |
ANDA |
ANDA208170 |
REMEDYREPACK INC. |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3415-5) |
| 76420-828-01 |
76420-828 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240702 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (76420-828-01) |
| 76420-828-12 |
76420-828 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240702 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
120 TABLET, FILM COATED in 1 BOTTLE (76420-828-12) |
| 76420-828-30 |
76420-828 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240702 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (76420-828-30) |
| 76420-828-60 |
76420-828 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240702 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (76420-828-60) |
| 76420-828-90 |
76420-828 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240702 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (76420-828-90) |
| 76420-829-01 |
76420-829 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240702 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
7.5 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (76420-829-01) |
| 76420-829-07 |
76420-829 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20250204 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
7.5 mg/1 |
7 TABLET, FILM COATED in 1 BOTTLE (76420-829-07) |
| 76420-829-12 |
76420-829 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240702 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
7.5 mg/1 |
120 TABLET, FILM COATED in 1 BOTTLE (76420-829-12) |
| 76420-829-30 |
76420-829 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240702 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
7.5 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (76420-829-30) |
| 76420-829-60 |
76420-829 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240702 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
7.5 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (76420-829-60) |
| 76420-829-90 |
76420-829 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240702 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
7.5 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (76420-829-90) |
| 76420-830-00 |
76420-830 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240702 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
1000 TABLET, FILM COATED in 1 BOTTLE (76420-830-00) |
| 76420-830-01 |
76420-830 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240702 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (76420-830-01) |
| 76420-830-05 |
76420-830 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240702 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
500 TABLET, FILM COATED in 1 BOTTLE (76420-830-05) |
| 76420-830-07 |
76420-830 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240702 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
7 TABLET, FILM COATED in 1 BOTTLE (76420-830-07) |
| 76420-830-12 |
76420-830 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240702 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
120 TABLET, FILM COATED in 1 BOTTLE (76420-830-12) |
| 76420-830-30 |
76420-830 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240702 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (76420-830-30) |