Oxybutynin Chloride
- Product NDC
- 63629-1354
- 11-digit product format
- 636291354
- Labeler code
- 63629
- Product ID
- 63629-1354_6f66dcc8-7f59-4203-9068-2be0f0544b46
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oxybutynin chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075079
- Marketing category
- ANDA
- Marketing start
- 1997-10-31
- 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 |
|---|
| 63629-1354-1 | 63629135401 | 30 TABLET in 1 BOTTLE (63629-1354-1) | 30 tablet | 2010-05-17 | 0000-00-00 | No | No | Current |
| 63629-1354-2 | 63629135402 | 100 TABLET in 1 BOTTLE (63629-1354-2) | 100 tablet | 2010-05-17 | 0000-00-00 | No | No | Current |
| 63629-1354-3 | 63629135403 | 20 TABLET in 1 BOTTLE (63629-1354-3) | 20 tablet | 2010-05-17 | 0000-00-00 | No | No | Current |
| 63629-1354-4 | 63629135404 | 60 TABLET in 1 BOTTLE, PLASTIC (63629-1354-4) | 60 tablet | 1997-10-31 | 0000-00-00 | No | No | Current |
| 63629-1354-5 | 63629135405 | 90 TABLET in 1 BOTTLE, PLASTIC (63629-1354-5) | 90 tablet | 1997-10-31 | 0000-00-00 | No | No | Current |
| 63629-1354-6 | 63629135406 | 42 TABLET in 1 BOTTLE (63629-1354-6) | 42 tablet | 2010-05-17 | 0000-00-00 | No | No | Current |
| 63629-1354-7 | 63629135407 | 15 TABLET in 1 BOTTLE (63629-1354-7) | 15 tablet | 2010-05-17 | 0000-00-00 | No | No | Current |
| 63629-1354-8 | 63629135408 | 180 TABLET in 1 BOTTLE (63629-1354-8) | 180 tablet | 2008-07-22 | 0000-00-00 | No | No | Current |