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OXYBUTYNIN CHLORIDE
OXYBUTYNIN CHLORIDE - 0121-0671-05 - (OXYBUTYNIN CHLORIDE)
Drug Information of OXYBUTYNIN CHLORIDE
| Product NDC: | 0121-0671 |
| Proprietary Name: | OXYBUTYNIN CHLORIDE |
| Non Proprietary Name: | OXYBUTYNIN CHLORIDE |
| Active Ingredient(s): | 5 mg/5mL & nbsp; OXYBUTYNIN CHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OXYBUTYNIN CHLORIDE
| Product NDC: | 0121-0671 |
| Labeler Name: | Pharmaceutical Associates, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075137 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19981218 |
Package Information of OXYBUTYNIN CHLORIDE
| Package NDC: | 0121-0671-05 |
| Package Description: | 4 TRAY in 1 CASE (0121-0671-05) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE |
NDC Information of OXYBUTYNIN CHLORIDE
| NDC Code | 0121-0671-05 |
| Proprietary Name | OXYBUTYNIN CHLORIDE |
| Package Description | 4 TRAY in 1 CASE (0121-0671-05) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE |
| Product NDC | 0121-0671 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | OXYBUTYNIN CHLORIDE |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 19981218 |
| Marketing Category Name | ANDA |
| Labeler Name | Pharmaceutical Associates, Inc. |
| Substance Name | OXYBUTYNIN CHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |
