Oxybutynin Chloride
- Product NDC
- 0615-7520
- 11-digit product format
- 006157520
- Labeler code
- 0615
- Product ID
- 0615-7520_6f42883f-b5f6-40a3-99bd-2603e61d2444
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oxybutynin chloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA076644
- Marketing category
- ANDA
- Marketing start
- 2006-11-10
- Marketing end
- 2020-04-30
- Substance
- OXYBUTYNIN CHLORIDE
- Active strength
- 10 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