oxybutynin chloride
- Product NDC
- 71205-667
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oxybutynin chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA207138
- Marketing category
- ANDA
- Substance
- OXYBUTYNIN CHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71205-667-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-30) | 2022-06-08 | | No | Historical |
| 71205-667-60 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-60) | 2022-06-08 | | No | Historical |
| 71205-667-90 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-90) | 2022-06-08 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| oxybutynin chloride | Proficient Rx LP | 2022-06-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |