| 68071-3475-4 |
68071-3475 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240923 |
N/A |
ANDA |
ANDA208170 |
NuCare Pharmaceuticals,Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
14 TABLET, FILM COATED in 1 BOTTLE (68071-3475-4) |
| 68071-3475-9 |
68071-3475 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20250114 |
N/A |
ANDA |
ANDA208170 |
NuCare Pharmaceuticals,Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (68071-3475-9) |
| 80425-0498-1 |
80425-0498 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20250320 |
N/A |
ANDA |
ANDA208170 |
Advanced Rx of Tennessee, LLC |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (80425-0498-1) |
| 80425-0498-2 |
80425-0498 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20250320 |
N/A |
ANDA |
ANDA208170 |
Advanced Rx of Tennessee, LLC |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (80425-0498-2) |
| 80425-0498-3 |
80425-0498 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20250320 |
N/A |
ANDA |
ANDA208170 |
Advanced Rx of Tennessee, LLC |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (80425-0498-3) |
| 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) |
| 85509-1014-3 |
85509-1014 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20250722 |
N/A |
ANDA |
ANDA208170 |
PHOENIX RX LLC |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (85509-1014-3) |
| 85509-1014-6 |
85509-1014 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20250722 |
N/A |
ANDA |
ANDA208170 |
PHOENIX RX LLC |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (85509-1014-6) |
| 85509-1014-9 |
85509-1014 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20250722 |
N/A |
ANDA |
ANDA208170 |
PHOENIX RX LLC |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (85509-1014-9) |