| 76420-456-60 |
76420-456 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20250813 |
N/A |
ANDA |
ANDA208170 |
ASCLEMED USA INC. |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (76420-456-60) |
| 76420-456-90 |
76420-456 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20250813 |
N/A |
ANDA |
ANDA208170 |
ASCLEMED USA INC. |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (76420-456-90) |
| 76420-456-01 |
76420-456 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20250813 |
N/A |
ANDA |
ANDA208170 |
ASCLEMED USA INC. |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
1 TABLET, FILM COATED in 1 BOTTLE (76420-456-01) |
| 76420-456-02 |
76420-456 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20250813 |
N/A |
ANDA |
ANDA208170 |
ASCLEMED USA INC. |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
2 TABLET, FILM COATED in 1 BOTTLE (76420-456-02) |
| 76420-456-04 |
76420-456 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20250813 |
N/A |
ANDA |
ANDA208170 |
ASCLEMED USA INC. |
CYCLOBENZAPRINE HYDROCHLORIDE |
10 mg/1 |
4 TABLET, FILM COATED in 1 BOTTLE (76420-456-04) |
| 72603-310-01 |
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 |
100 TABLET, FILM COATED in 1 BOTTLE (72603-310-01) |
| 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) |
| 71205-356-15 |
71205-356 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20210720 |
N/A |
ANDA |
ANDA208170 |
Proficient Rx LP |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
15 TABLET, FILM COATED in 1 BOTTLE (71205-356-15) |
| 71205-356-20 |
71205-356 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20230406 |
N/A |
ANDA |
ANDA208170 |
Proficient Rx LP |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
20 TABLET, FILM COATED in 1 BOTTLE (71205-356-20) |
| 71205-356-21 |
71205-356 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20230406 |
N/A |
ANDA |
ANDA208170 |
Proficient Rx LP |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
21 TABLET, FILM COATED in 1 BOTTLE (71205-356-21) |
| 71205-356-30 |
71205-356 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20191101 |
N/A |
ANDA |
ANDA208170 |
Proficient Rx LP |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (71205-356-30) |
| 71205-356-40 |
71205-356 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20240108 |
N/A |
ANDA |
ANDA208170 |
Proficient Rx LP |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
40 TABLET, FILM COATED in 1 BOTTLE (71205-356-40) |
| 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) |
| 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) |
| 70518-2611-3 |
70518-2611 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20241002 |
N/A |
ANDA |
ANDA208170 |
REMEDYREPACK INC. |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2611-3) |
| 70518-2611-4 |
70518-2611 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20241108 |
N/A |
ANDA |
ANDA208170 |
REMEDYREPACK INC. |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2611-4) |
| 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) |
| 71205-356-60 |
71205-356 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20191101 |
N/A |
ANDA |
ANDA208170 |
Proficient Rx LP |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (71205-356-60) |
| 71205-356-90 |
71205-356 |
HUMAN PRESCRIPTION DRUG |
CYCLOBENZAPRINE HYDROCHLORIDE |
cyclobenzaprine hydrochloride |
TABLET, FILM COATED |
ORAL |
20191101 |
N/A |
ANDA |
ANDA208170 |
Proficient Rx LP |
CYCLOBENZAPRINE HYDROCHLORIDE |
5 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (71205-356-90) |