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CYCLOBENZAPRINE HYROCHLORIDE
CYCLOBENZAPRINE HYROCHLORIDE - 76519-1000-2 - (CYCLOBENZAPRINE HYDROCHLORIDE)
Drug Information of CYCLOBENZAPRINE HYROCHLORIDE
| Product NDC: | 76519-1000 |
| Proprietary Name: | CYCLOBENZAPRINE HYROCHLORIDE |
| Non Proprietary Name: | CYCLOBENZAPRINE HYDROCHLORIDE |
| Active Ingredient(s): | 7.5 mg/1 & nbsp; CYCLOBENZAPRINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CYCLOBENZAPRINE HYROCHLORIDE
| Product NDC: | 76519-1000 |
| Labeler Name: | H.J. Harkins Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078722 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110829 |
Package Information of CYCLOBENZAPRINE HYROCHLORIDE
| Package NDC: | 76519-1000-2 |
| Package Description: | 20 TABLET in 1 BOTTLE (76519-1000-2) |
NDC Information of CYCLOBENZAPRINE HYROCHLORIDE
| NDC Code | 76519-1000-2 |
| Proprietary Name | CYCLOBENZAPRINE HYROCHLORIDE |
| Package Description | 20 TABLET in 1 BOTTLE (76519-1000-2) |
| Product NDC | 76519-1000 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CYCLOBENZAPRINE HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110829 |
| Marketing Category Name | ANDA |
| Labeler Name | H.J. Harkins Company, Inc. |
| Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
| Strength Number | 7.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |
