| 72603-310-02 |
72603-310 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine Hydrochloride |
Cyclobenzaprine Hydrochloride |
TABLET, FILM COATED |
ORAL |
20241101 |
N/A |
ANDA |
ANDA208170 |
NORTHSTAR RX LLC |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
500 TABLET, FILM COATED in 1 BOTTLE (72603-310-02) |
| 76420-030-01 |
76420-030 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20200619 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (76420-030-01) |
| 76420-030-05 |
76420-030 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20200619 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
500 TABLET, FILM COATED in 1 BOTTLE (76420-030-05) |
| 76420-030-12 |
76420-030 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20220729 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
120 TABLET, FILM COATED in 1 BOTTLE (76420-030-12) |
| 76420-030-30 |
76420-030 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20200619 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (76420-030-30) |
| 76420-030-60 |
76420-030 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20200619 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (76420-030-60) |
| 76420-030-90 |
76420-030 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20200619 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (76420-030-90) |
| 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) |
| 72603-311-01 |
72603-311 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine Hydrochloride |
Cyclobenzaprine Hydrochloride |
TABLET, FILM COATED |
ORAL |
20241101 |
N/A |
ANDA |
ANDA208170 |
NORTHSTAR RX LLC |
CYCLOBENZAPRINE HYDROCHLORIDE |
7.5 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (72603-311-01) |
| 76420-265-10 |
76420-265 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20220901 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
7.5 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (76420-265-10) |
| 76420-265-30 |
76420-265 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20220901 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
7.5 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (76420-265-30) |
| 76420-265-60 |
76420-265 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20220901 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
7.5 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (76420-265-60) |
| 76420-265-90 |
76420-265 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20220901 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
7.5 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (76420-265-90) |
| 68071-4655-2 |
68071-4655 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20181207 |
N/A |
ANDA |
ANDA208170 |
NuCare Pharmaceutuicals,Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
12 TABLET, FILM COATED in 1 BOTTLE (68071-4655-2) |
| 52817-331-10 |
52817-331 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20170531 |
N/A |
ANDA |
ANDA208170 |
TruPharma LLC |
CYCLOBENZAPRINE HYDROCHLORIDE |
7.5 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (52817-331-10) |
| 71205-065-10 |
71205-065 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20180702 |
N/A |
ANDA |
ANDA208170 |
Proficient Rx LP |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
10 TABLET, FILM COATED in 1 BOTTLE (71205-065-10) |
| 50090-4722-0 |
50090-4722 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20191115 |
N/A |
ANDA |
ANDA208170 |
A-S Medication Solutions |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
15 TABLET, FILM COATED in 1 BOTTLE (50090-4722-0) |
| 51655-592-20 |
51655-592 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20230131 |
N/A |
ANDA |
ANDA208170 |
Northwind Health Company, LLC |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-20) |