Oxybutynin Chloride
- Product NDC
- 63629-2245
- 11-digit product format
- 636292245
- Labeler code
- 63629
- Product ID
- 63629-2245_9a2ab665-aed6-4f63-8bca-14303ab05a49
- 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
- 2023-12-31
- 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 |
|---|
| 63629-2245-1 | 63629224501 | 1000 TABLET in 1 BOTTLE, PLASTIC (63629-2245-1) | 1000 tablet | 2021-03-24 | 0000-00-00 | No | No | Current |