Oxybutynin Chloride
- Product NDC
- 71930-051
- 11-digit product format
- 719300051
- Labeler code
- 71930
- Product ID
- 71930-051_8b369b71-fbec-b41f-e053-2a95a90a4530
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxybutynin Chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Eywa Pharma Inc
- Application
- ANDA211062
- Marketing category
- ANDA
- Marketing start
- 2019-07-15
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71930-051-12 | 71930005112 | 100 TABLET in 1 BOTTLE (71930-051-12) | 100 tablet | 2019-07-15 | 0000-00-00 | No | No | Current |
| 71930-051-13 | 71930005113 | 1000 TABLET in 1 BOTTLE (71930-051-13) | 1000 tablet | 2019-07-15 | 0000-00-00 | No | No | Current |
| 71930-051-52 | 71930005152 | 500 TABLET in 1 BOTTLE (71930-051-52) | 500 tablet | 2019-07-15 | 0000-00-00 | No | No | Current |