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Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride - 0781-5032-64 - (Cyclobenzaprine Hydrochloride)
Drug Information of Cyclobenzaprine Hydrochloride
| Product NDC: | 0781-5032 |
| Proprietary Name: | Cyclobenzaprine Hydrochloride |
| Non Proprietary Name: | Cyclobenzaprine Hydrochloride |
| Active Ingredient(s): | 5 mg/1 & nbsp; Cyclobenzaprine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cyclobenzaprine Hydrochloride
| Product NDC: | 0781-5032 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072854 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060206 |
Package Information of Cyclobenzaprine Hydrochloride
| Package NDC: | 0781-5032-64 |
| Package Description: | 10 TABLET, FILM COATED in 1 BLISTER PACK (0781-5032-64) |
NDC Information of Cyclobenzaprine Hydrochloride
| NDC Code | 0781-5032-64 |
| Proprietary Name | Cyclobenzaprine Hydrochloride |
| Package Description | 10 TABLET, FILM COATED in 1 BLISTER PACK (0781-5032-64) |
| Product NDC | 0781-5032 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cyclobenzaprine Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20060206 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |
