Oxybutynin Chloride
- Product NDC
- 50090-2049
- 11-digit product format
- 500902049
- Labeler code
- 50090
- Product ID
- 50090-2049_92abec07-205a-4e21-bcda-0bacb901ccd1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oxybutynin chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2049-0 | 50090204900 | 30 TABLET in 1 BOTTLE (50090-2049-0) | 30 tablet | 2015-09-30 | 0000-00-00 | No | No | Current |
| 50090-2049-1 | 50090204901 | 100 TABLET in 1 BOTTLE (50090-2049-1) | 100 tablet | 2015-09-30 | 0000-00-00 | No | No | Current |
| 50090-2049-3 | 50090204903 | 90 TABLET in 1 BOTTLE (50090-2049-3) | 90 tablet | 2015-09-30 | 0000-00-00 | No | No | Current |