oxybutynin chloride
- Product NDC
- 63629-9689
- 11-digit product format
- 636299689
- Labeler code
- 63629
- Product ID
- 63629-9689_c450b483-367b-4480-b955-7fef7ac25ba4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oxybutynin chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA207138
- Marketing category
- ANDA
- Marketing start
- 2016-12-14
- Substance
- OXYBUTYNIN CHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| L9F3D9RENQ | OXYBUTYNIN CHLORIDE | 1508-65-2 | OXYBUTYNIN CHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 63629-9689-1 | 63629968901 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-9689-1) | 2023-06-21 | No | No | Historical |
| 63629-9689-2 | 63629968902 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-9689-2) | 2023-06-21 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| oxybutynin chloride | Bryant Ranch Prepack | 2026-05-14 | HUMAN PRESCRIPTION DRUG LABEL | 102 |