Oxybutynin 5 mg / 1 Tablet 500 Tablet, Film Coated, Extended Release
Reference details for licensed healthcare facility review and verification.
| NDC 11 | 68382-0255-05 |
|---|---|
| Product NDC | 68382-0255 |
| Generic Drug Name | oxybutynin |
| Brand Name | oxybutynin |
| Manufacturer | Zydus Pharmaceuticals USA Inc. |
| Strength | 5 mg / 1 |
| Dosage Form | Tablet |
| Drug Type | Oral |
| Package Quantity | 500 Tablet, Film Coated, Extended Release |
| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-255-05) |
| Active Ingredients | Oxybutynin Chloride |
| Marketing Category | ANDA |
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NDC snapshot
oxybutynin 5 mg / 1 Tablet is tracked under NDC 68382-0255-05 and rolls up into product family 68382-0255. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.
- Package configuration: 500 Tablet, Film Coated, Extended Release.
- Manufacturer: Zydus Pharmaceuticals USA Inc..
- Dosage form: Tablet.
- Family size: 6 indexed presentations.
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Official references
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Alternate presentations in this family
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Potential alternatives with matching presentation
Open the comparison hub or review package-level listings from 2 product-NDC families with matching normalized presentation details. Review each product detail page before treating any item as a true alternative.
View Potential Alternative Huboxybutynin 5 mg / 1 Tablet extended release 500 Tablet, Film Coated, Extended Release Bottle2 package-level listings in the comparison hub.Sample package-level pages in this comparison set
Oxybutynin 5 mg / 1 Tablet 500 Tablet, Film Coated, Extended Release, NDC 68382-0255-05, is a Zydus Pharmaceuticals USA Inc. 5 mg / 1 tablet presentation packaged as 500 Tablet, Film Coated, Extended Release.
NDC search formats
- Canonical NDC 11: 68382-0255-05
- Digits-only NDC 11: 68382025505
- Possible 10-digit display formats: 68382-255-05 (6838225505), 68382-0255-5 (6838202555)
Multiple 10-digit display-format aliases can map to the same stored 11-digit billing NDC, so these are shown as search aliases rather than a single asserted package format.
Helpful product links
- Search by brand name: oxybutynin
- NDC 11: 68382-0255-05
- Product family NDC: 68382-0255
- Other package sizes in this family: 10 Blister Pack, 100 Tablet, Film Coated, Extended Release, 30 Tablet, Film Coated, Extended Release, 60 Tablet, Film Coated, Extended Release, 90 Tablet, Film Coated, Extended Release
- Compare related presentations: Oxybutynin 5 mg / 1 Tablet 10 Blister Pack, Oxybutynin 5 mg / 1 Tablet 100 Tablet, Film Coated, Extended Release, Oxybutynin 5 mg / 1 Tablet 30 Tablet, Film Coated, Extended Release, Oxybutynin 5 mg / 1 Tablet 60 Tablet, Film Coated, Extended Release, Oxybutynin 5 mg / 1 Tablet 90 Tablet, Film Coated, Extended Release
- VA classification code: GU201
- VA classification code description: ANTISPASMODICS,URINARY
- CMOP ID: O0090
- VUID: 4013406