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Oxybutynin Chloride
Oxybutynin Chloride - 51079-722-63 - (oxybutynin chloride)
Drug Information of Oxybutynin Chloride
| Product NDC: | 51079-722 |
| Proprietary Name: | Oxybutynin Chloride |
| Non Proprietary Name: | oxybutynin chloride |
| Active Ingredient(s): | 5 mg/1 & nbsp; oxybutynin chloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oxybutynin Chloride
| Product NDC: | 51079-722 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076702 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110114 |
Package Information of Oxybutynin Chloride
| Package NDC: | 51079-722-63 |
| Package Description: | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 DOSE PACK (51079-722-63) |
NDC Information of Oxybutynin Chloride
| NDC Code | 51079-722-63 |
| Proprietary Name | Oxybutynin Chloride |
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 DOSE PACK (51079-722-63) |
| Product NDC | 51079-722 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | oxybutynin chloride |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20110114 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | OXYBUTYNIN CHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |
