Cyclobenzaprine Hydrochloride is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Apotheca Inc.. The primary component is Cyclobenzaprine Hydrochloride.
Product ID | 12634-528_27fe4bb9-282f-42ca-e054-00144ff88e88 |
NDC | 12634-528 |
Product Type | Human Prescription Drug |
Proprietary Name | Cyclobenzaprine Hydrochloride |
Generic Name | Cyclobenzaprine Hydrochloride |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2012-04-02 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA090478 |
Labeler Name | Apotheca Inc. |
Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
Active Ingredient Strength | 10 mg/1 |
Pharm Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2012-04-02 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA090478 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-04-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090478 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-04-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090478 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-04-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090478 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-04-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090478 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2015-12-28 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090478 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-04-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090478 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-04-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090478 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-04-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090478 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-04-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090478 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-04-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090478 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-04-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090478 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-04-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090478 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-04-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090478 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-04-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090478 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-04-02 |
Marketing End Date | 2015-12-28 |
Marketing Category | ANDA |
Application Number | ANDA090478 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-04-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090478 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-04-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090478 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-04-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090478 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-04-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090478 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-04-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090478 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-04-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090478 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-04-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090478 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-04-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090478 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-04-02 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
CYCLOBENZAPRINE HYDROCHLORIDE | 10 mg/1 |
SPL SET ID: | 27327397-3ff7-6e43-e054-00144ff88e88 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
0093-1920 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
0093-1921 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
0093-3420 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
0093-3421 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
0093-3422 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
0115-1436 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
0115-1437 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
0179-0057 | cyclobenzaprine hydrochloride | cyclobenzaprine hydrochloride |
0179-0189 | cyclobenzaprine hydrochloride | cyclobenzaprine hydrochloride |
0378-0751 | Cyclobenzaprine Hydrochloride | cyclobenzaprine hydrochloride |
0378-0761 | Cyclobenzaprine Hydrochloride | cyclobenzaprine hydrochloride |
0378-0771 | Cyclobenzaprine Hydrochloride | cyclobenzaprine hydrochloride |
0440-1350 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
0440-7350 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
0591-3256 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
0591-3330 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
0591-5658 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
0615-3520 | Cyclobenzaprine Hydrochloride | cyclobenzaprine hydrochloride |
0615-7528 | Cyclobenzaprine Hydrochloride | cyclobenzaprine hydrochloride |
0615-8084 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine |
0615-8182 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
68071-3149 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
68071-1983 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
68071-1961 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
68071-1998 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
68071-3154 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
68071-3377 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
68071-3150 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
68071-3390 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
68071-4076 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
68071-4415 | Cyclobenzaprine hydrochloride | Cyclobenzaprine hydrochloride |
68071-4502 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
68071-4655 | CYCLOBENZAPRINE HYDROCHLORIDE | CYCLOBENZAPRINE HYDROCHLORIDE |
68071-4826 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
68084-753 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
68258-7150 | CYCLOBENZAPRINE HYDROCHLORIDE | CYCLOBENZAPRINE HYDROCHLORIDE |
68258-7013 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
68387-500 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
68387-502 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
68645-518 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
68645-517 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
68788-6375 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
68788-7398 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
68788-9069 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
68788-7131 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
68788-9508 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
68788-9295 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
68788-9967 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
69097-846 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |
69097-845 | Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride |