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NDC 68382-0255-06 oxybutynin 5 mg/1 Details
oxybutynin 5 mg/1
oxybutynin is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Zydus Pharmaceuticals USA Inc.. The primary component is OXYBUTYNIN CHLORIDE.
MedlinePlus Drug Summary
Oxybutynin is used to treat overactive bladder (a condition in which the bladder muscles contract uncontrollably and cause frequent urination, urgent need to urinate, and inability to control urination) in certain adults and children. Oxybutynin is also used as an extended-release tablet to control bladder muscles in adults and children 6 years of age and older with spina bifida (a disability that occurs when the spinal cord does not close properly before birth), or other nervous system conditions that affect the bladder muscles. Oxybutynin is in a class of medications called anticholinergics/antimuscarinics. It works by relaxing the bladder muscles.
Related Packages: 68382-0255-06Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Oxybutynin
Product Information
| NDC | 68382-0255 |
|---|---|
| Product ID | 68382-255_f54e4d4e-91be-4e10-a446-57ed5e1843a1 |
| Associated GPIs | 54100045207520 |
| GCN Sequence Number | 041046 |
| GCN Sequence Number Description | oxybutynin chloride TAB ER 24 5 MG ORAL |
| HIC3 | R1A |
| HIC3 Description | URINARY TRACT ANTISPASMODIC/ANTIINCONTINENCE AGENT |
| GCN | 19388 |
| HICL Sequence Number | 002048 |
| HICL Sequence Number Description | OXYBUTYNIN CHLORIDE |
| Brand/Generic | Generic |
| Proprietary Name | oxybutynin |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | oxybutynin |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
| Route | ORAL |
| Active Ingredient Strength | 5 |
| Active Ingredient Units | mg/1 |
| Substance Name | OXYBUTYNIN CHLORIDE |
| Labeler Name | Zydus Pharmaceuticals USA Inc. |
| Pharmaceutical Class | Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA202332 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 68382-0255-06 (68382025506)
| NDC Package Code | 68382-255-06 |
|---|---|
| Billing NDC | 68382025506 |
| Package | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-255-06) |
| Marketing Start Date | 2017-08-10 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |