Oxybutynin Chloride
- Product NDC
- 68084-400
- 11-digit product format
- 680840400
- Labeler code
- 68084
- Product ID
- 68084-400_e711c86c-6f55-564d-e053-2995a90ad0e3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oxybutynin chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA075079
- Marketing category
- ANDA
- Marketing start
- 2009-08-20
- Marketing end
- 2023-06-30
- 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 |
|---|
| 68084-400-01 | 68084040001 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-400-01) > 1 TABLET in 1 BLISTER PACK (68084-400-11) | 100 blister pack | 2009-08-20 | 0000-00-00 | No | No | Current |