Oxybutynin Chloride
- Product NDC
- 71335-0669
- 11-digit product format
- 713350669
- Labeler code
- 71335
- Product ID
- 71335-0669_fdb134dd-90dc-44d4-8c41-8af97fb6b1e9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxybutynin Chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078503
- Marketing category
- ANDA
- Marketing start
- 2009-03-01
- Marketing end
- 0000-00-00
- Substance
- OXYBUTYNIN CHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 71335-0669-1 | 71335066901 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0669-1) | 2018-01-30 | 0000-00-00 | No | No | Current |
| 71335-0669-2 | 71335066902 | 18 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0669-2) | 2018-01-30 | 0000-00-00 | No | No | Current |
| 71335-0669-3 | 71335066903 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0669-3) | 2018-01-30 | 0000-00-00 | No | No | Current |
| 71335-0669-4 | 71335066904 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0669-4) | 2018-01-30 | 0000-00-00 | No | No | Current |