Oxybutynin Chloride
- Product NDC
- 55154-0657
- 11-digit product format
- 551540657
- Labeler code
- 55154
- Product ID
- 55154-0657_7d682d9c-405a-4711-baf0-7da812a087c1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxybutynin Chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA071655
- Marketing category
- ANDA
- Marketing start
- 2004-02-03
- 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 |
|---|
| 55154-0657-0 | 55154065700 | 10 BLISTER PACK in 1 BAG (55154-0657-0) > 1 TABLET in 1 BLISTER PACK | 10 blister pack | 2004-02-03 | 0000-00-00 | No | No | Current |