oxybutynin chloride
- Product NDC
- 70518-3032
- 11-digit product format
- 705183032
- Labeler code
- 70518
- Product ID
- 70518-3032_bc7af2a5-f30c-80fb-e053-2995a90a4b79
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oxybutynin chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA207138
- Marketing category
- ANDA
- Marketing start
- 2021-02-26
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3032-0 | 70518303200 | 100 POUCH in 1 BOX (70518-3032-0) > 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-3032-1) | 100 pouch | 2021-02-26 | 0000-00-00 | No | No | Current |