| 76420-011-04 |
76420-011 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20250411 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
4 TABLET, FILM COATED in 1 BOTTLE (76420-011-04) |
| 76420-011-05 |
76420-011 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20241224 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
5 TABLET, FILM COATED in 1 BOTTLE (76420-011-05) |
| 76420-011-01 |
76420-011 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20200123 |
N/A |
ANDA |
ANDA208170 |
Asclemed USA, Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
1 TABLET, FILM COATED in 1 BOTTLE (76420-011-01) |
| 72603-312-01 |
72603-312 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine Hydrochloride |
Cyclobenzaprine Hydrochloride |
TABLET, FILM COATED |
ORAL |
20241101 |
N/A |
ANDA |
ANDA208170 |
NORTHSTAR RX LLC |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (72603-312-01) |
| 72603-312-02 |
72603-312 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine Hydrochloride |
Cyclobenzaprine Hydrochloride |
TABLET, FILM COATED |
ORAL |
20241101 |
N/A |
ANDA |
ANDA208170 |
NORTHSTAR RX LLC |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
500 TABLET, FILM COATED in 1 BOTTLE (72603-312-02) |
| 72603-312-03 |
72603-312 |
HUMAN PRESCRIPTION DRUG |
Cyclobenzaprine Hydrochloride |
Cyclobenzaprine Hydrochloride |
TABLET, FILM COATED |
ORAL |
20241101 |
N/A |
ANDA |
ANDA208170 |
NORTHSTAR RX LLC |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
1000 TABLET, FILM COATED in 1 BOTTLE (72603-312-03) |
| 51655-818-52 |
51655-818 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20230228 |
N/A |
ANDA |
ANDA208170 |
Northwind Health Company, LLC |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-818-52) |
| 51655-818-53 |
51655-818 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20230824 |
N/A |
ANDA |
ANDA208170 |
Northwind Health Company, LLC |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-818-53) |
| 51655-818-26 |
51655-818 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20230131 |
N/A |
ANDA |
ANDA208170 |
Northwind Health Company, LLC |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-818-26) |
| 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) |
| 76420-030-60 |
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) |
| 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) |
| 76420-030-01 |
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) |
| 76420-030-30 |
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) |
| 68071-3462-2 |
68071-3462 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20230719 |
N/A |
ANDA |
ANDA208170 |
NuCare Pharmaceuticals,Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
20 TABLET, FILM COATED in 1 BOTTLE (68071-3462-2) |
| 68071-3475-2 |
68071-3475 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20230801 |
N/A |
ANDA |
ANDA208170 |
NuCare Pharmaceuticals,Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
12 TABLET, FILM COATED in 1 BOTTLE (68071-3475-2) |
| 68071-3475-3 |
68071-3475 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20230801 |
N/A |
ANDA |
ANDA208170 |
NuCare Pharmaceuticals,Inc. |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (68071-3475-3) |
| 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) |