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CYCLOBENZAPRINE HYDROCHLORIDE
CYCLOBENZAPRINE HYDROCHLORIDE - 68084-397-01 - (CYCLOBENZAPRINE HYDROCHLORIDE)
Drug Information of CYCLOBENZAPRINE HYDROCHLORIDE
| Product NDC: | 68084-397 |
| Proprietary Name: | CYCLOBENZAPRINE HYDROCHLORIDE |
| Non Proprietary Name: | CYCLOBENZAPRINE HYDROCHLORIDE |
| Active Ingredient(s): | 10 mg/1 & nbsp; CYCLOBENZAPRINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CYCLOBENZAPRINE HYDROCHLORIDE
| Product NDC: | 68084-397 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077797 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091014 |
Package Information of CYCLOBENZAPRINE HYDROCHLORIDE
| Package NDC: | 68084-397-01 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (68084-397-01) > 10 TABLET in 1 BLISTER PACK (68084-397-11) |
NDC Information of CYCLOBENZAPRINE HYDROCHLORIDE
| NDC Code | 68084-397-01 |
| Proprietary Name | CYCLOBENZAPRINE HYDROCHLORIDE |
| Package Description | 10 BLISTER PACK in 1 CARTON (68084-397-01) > 10 TABLET in 1 BLISTER PACK (68084-397-11) |
| Product NDC | 68084-397 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CYCLOBENZAPRINE HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20091014 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |
