oxybutynin 10 mg/1
oxybutynin · TABLET, FILM COATED, EXTENDED RELEASE · A-S Medication Solutions
oxybutynin is a tablet, film coated, extended release containing oxybutynin at 10 mg/1, taken oral. Manufactured by A-S Medication Solutions.
Key Facts
- Brand Name
- oxybutynin
- Generic Name
- oxybutynin
- NDC Code (Product)
50090-5353- Manufacturer
- A-S Medication Solutions
- Strength
- 10 mg/1
- Dosage Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA202332
- Marketing Start
- 08/10/2017
Recall History
Zydus Pharmaceuticals (USA) Inc
Failed Dissolution Specifications-out-of-specification (OOS) test results observed for dissolution at the 6 month long term time point.
Zydus Pharmaceuticals (USA) Inc
Failed Dissolution Specifications
Zydus Pharmaceuticals (USA) Inc
Failed Dissolution Specifications-out-of-specification (OOS) test results observed for dissolution at the 6 month long term time point.
Actavis
Subpotent Drug: Drug potency was compromised during shipment.
Zydus Pharmaceuticals (USA) Inc
Failed Dissolution Specifications-out-of-specification (OOS) test results observed for dissolution at the 6 month long term time point.
KVK-Tech, Inc.
Labeling: Wrong bar code
AVKARE Inc.
Failed Dissolution Specifications
Aidapak Services, LLC
Labeling: Label Mixup: OXYBUTYNIN CHLORIDE, Tablet, 5 mg may have potentially been mislabeled as one of the following drugs: FLECAINIDE ACETATE, Tablet, 100 mg, NDC 00054001125, Pedigree: AD56847_4, EXP: 5/21/2014; SODIUM CHLORIDE, Tablet, 1 gm, NDC 00223176001, Pedigree: W003792, EXP: 6/27/2014; VARENICLINE, Tablet, 0.5 mg, NDC 00069046856, Pedigree: AD22616_1, EXP: 5/2/2014.
Lannett Company Inc.
Failed Dissolution Specifications
Aidapak Services, LLC
Labeling: Label Mixup: OXYBUTYNIN CHLORIDE, Tablet, 2.5 mg (1/2 of 5 mg) may have potentially been mislabeled as the following drug: PIMOZIDE, Tablet, 1 mg (1/2 of 2 mg), NDC 57844018701, Pedigree: AD73525_61, EXP: 5/30/2014.
Frequently Asked Questions
What is oxybutynin used for?
oxybutynin contains oxybutynin. It is a tablet, film coated, extended release taken oral. Consult your doctor for specific uses.
Is oxybutynin a controlled substance?
oxybutynin is not classified as a controlled substance by the DEA.
What is the generic name for oxybutynin?
The generic name for oxybutynin is oxybutynin. There are 11 other brand versions of oxybutynin.
What is the NDC code for oxybutynin 10 mg/1?
The NDC (National Drug Code) for oxybutynin 10 mg/1 is 50090-5353, listed by A-S Medication Solutions.
Other oxybutynin Dosages
Other Oxybutynin Brands
See all →- oxybutynin chloride10 mg/172789-049
- Oxybutynin Chloride10 mg/172888-031
- oxybutynin chloride15 mg/116729-319
- Oxybutynin Chloride Extended Release5 mg/143353-282
- Oxybutynin Chloride5 mg/143353-978
- OXYBUTYNIN CHLORIDE5 mg/150090-6638
- Oxybutynin Chloride5 mg/5mL54838-510
- oxybutynin chloride5 mg/162135-507
- Oxybutynin Chloride5 mg/170518-2640
- Oxybutynin Chloride5 mg/171335-0519
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)