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OXYBUTYNIN CHLORIDE
OXYBUTYNIN CHLORIDE - 0093-5208-01 - (OXYBUTYNIN CHLORIDE)
Drug Information of OXYBUTYNIN CHLORIDE
| Product NDC: | 0093-5208 |
| Proprietary Name: | OXYBUTYNIN CHLORIDE |
| Non Proprietary Name: | OXYBUTYNIN CHLORIDE |
| Active Ingredient(s): | 15 mg/1 & nbsp; OXYBUTYNIN CHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OXYBUTYNIN CHLORIDE
| Product NDC: | 0093-5208 |
| Labeler Name: | TEVA Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076745 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20061110 |
Package Information of OXYBUTYNIN CHLORIDE
| Package NDC: | 0093-5208-01 |
| Package Description: | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0093-5208-01) |
NDC Information of OXYBUTYNIN CHLORIDE
| NDC Code | 0093-5208-01 |
| Proprietary Name | OXYBUTYNIN CHLORIDE |
| Package Description | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0093-5208-01) |
| Product NDC | 0093-5208 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | OXYBUTYNIN CHLORIDE |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20061110 |
| Marketing Category Name | ANDA |
| Labeler Name | TEVA Pharmaceuticals USA Inc |
| Substance Name | OXYBUTYNIN CHLORIDE |
| Strength Number | 15 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |
