Oxybutynin Chloride
- Product NDC
- 0615-3512
- 11-digit product format
- 006153512
- Labeler code
- 0615
- Product ID
- 0615-3512_6905c0e0-8272-4436-97ea-6ed581c9e533
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxybutynin Chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA075079
- Marketing category
- ANDA
- Marketing start
- 2012-10-30
- Marketing end
- 2024-04-30
- 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 |
|---|
| 0615-3512-39 | 00615351239 | 30 TABLET in 1 BLISTER PACK (0615-3512-39) | 30 tablet | 2012-10-30 | 0000-00-00 | No | No | Current |