Oxytrol For Women
- Product NDC
- 52544-166
- 11-digit product format
- 525440166
- Labeler code
- 52544
- Product ID
- 52544-166_bc5775a5-41f9-4b68-a99a-7c30744d04f3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- oxybutynin
- Dosage form
- PATCH
- Route
- TRANSDERMAL
- Labeler
- Actavis Pharma, Inc.
- Application
- NDA202211
- Marketing category
- NDA
- Marketing start
- 2016-01-01
- Marketing end
- 2020-01-31
- Substance
- OXYBUTYNIN
- Active strength
- 4 mg/d
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 52544-166-04 | EA - Each | 52544-166 | 1d9b0372-7f91-4f16-992f-2a875a427fb0 | 1 | 2016-09-02 |
| 52544-166-08 | EA - Each | 52544-166 | d974b39b-5773-4546-8516-237e6ce398ea | 1 | 2016-09-02 |
| 52544-166-54 | EA - Each | 52544-166 | cc41de91-c574-4e85-9cae-a7a541857eef | 1 | 2016-09-02 |