Product NDC: | 63629-1564 |
Proprietary Name: | Orphenadrine Citrate |
Non Proprietary Name: | Orphenadrine Citrate |
Active Ingredient(s): | 100 mg/1 & nbsp; Orphenadrine Citrate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63629-1564 |
Labeler Name: | Bryant Ranch Prepack |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040284 |
Marketing Category: | ANDA |
Start Marketing Date: | 19980619 |
Package NDC: | 63629-1564-3 |
Package Description: | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1564-3) |
NDC Code | 63629-1564-3 |
Proprietary Name | Orphenadrine Citrate |
Package Description | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1564-3) |
Product NDC | 63629-1564 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Orphenadrine Citrate |
Dosage Form Name | TABLET, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 19980619 |
Marketing Category Name | ANDA |
Labeler Name | Bryant Ranch Prepack |
Substance Name | ORPHENADRINE CITRATE |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |