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AMRIX
AMRIX - 21695-723-14 - (Cyclobenzaprine Hydrochloride)
Drug Information of AMRIX
| Product NDC: | 21695-723 |
| Proprietary Name: | AMRIX |
| Non Proprietary Name: | Cyclobenzaprine Hydrochloride |
| Active Ingredient(s): | 15 mg/1 & nbsp; Cyclobenzaprine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AMRIX
| Product NDC: | 21695-723 |
| Labeler Name: | Rebel Distributors Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021777 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20071001 |
Package Information of AMRIX
| Package NDC: | 21695-723-14 |
| Package Description: | 14 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (21695-723-14) |
NDC Information of AMRIX
| NDC Code | 21695-723-14 |
| Proprietary Name | AMRIX |
| Package Description | 14 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (21695-723-14) |
| Product NDC | 21695-723 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cyclobenzaprine Hydrochloride |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20071001 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp. |
| Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
| Strength Number | 15 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |
