Oxybutynin Chloride
- Product NDC
- 0904-2821
- 11-digit product format
- 009042821
- Labeler code
- 0904
- Product ID
- 0904-2821_1f8365ae-b793-48cb-a0d0-369d8c6a5f1b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxybutynin Chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA071655
- Marketing category
- ANDA
- Marketing start
- 2004-02-03
- Marketing end
- 2023-09-30
- 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
- 0000-00-00
- 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 |
|---|
| 0904-2821-61 | 00904282161 | 100 BLISTER PACK in 1 CARTON (0904-2821-61) > 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2004-02-03 | 2023-09-30 | No | No | Current |