oxybutynin chloride
- Product NDC
- 68788-7109
- 11-digit product format
- 687887109
- Labeler code
- 68788
- Product ID
- 68788-7109_aa57e53b-cbc0-4e2a-823a-c64b0cd8d368
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oxybutynin chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA207138
- Marketing category
- ANDA
- Marketing start
- 2018-03-08
- Marketing end
- 0000-00-00
- Substance
- OXYBUTYNIN CHLORIDE
- Active strength
- 15 mg/1
- Pharmacologic classes
- Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7109-1 | 68788710901 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7109-1) | 2018-03-08 | 0000-00-00 | No | No | Current |
| 68788-7109-2 | 68788710902 | 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7109-2) | 2018-03-08 | 0000-00-00 | No | No | Current |
| 68788-7109-3 | 68788710903 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7109-3) | 2018-03-08 | 0000-00-00 | No | No | Current |
| 68788-7109-6 | 68788710906 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7109-6) | 2018-03-08 | 0000-00-00 | No | No | Current |
| 68788-7109-9 | 68788710909 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7109-9) | 2018-03-08 | 0000-00-00 | No | No | Current |