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CYCLOBENZAPRINE HYDROCHLORIDE
CYCLOBENZAPRINE HYDROCHLORIDE - 76218-1219-1 - (CYCLOBENZAPRINE HYDROCHLORIDE)
Drug Information of CYCLOBENZAPRINE HYDROCHLORIDE
| Product NDC: | 76218-1219 |
| Proprietary Name: | CYCLOBENZAPRINE HYDROCHLORIDE |
| 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 HYDROCHLORIDE
| Product NDC: | 76218-1219 |
| Labeler Name: | KLE 2, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078722 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110829 |
Package Information of CYCLOBENZAPRINE HYDROCHLORIDE
| Package NDC: | 76218-1219-1 |
| Package Description: | 1000 TABLET in 1 BOTTLE (76218-1219-1) |
NDC Information of CYCLOBENZAPRINE HYDROCHLORIDE
| NDC Code | 76218-1219-1 |
| Proprietary Name | CYCLOBENZAPRINE HYDROCHLORIDE |
| Package Description | 1000 TABLET in 1 BOTTLE (76218-1219-1) |
| Product NDC | 76218-1219 |
| 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 | KLE 2, Inc. |
| Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
| Strength Number | 7.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |
