oxybutynin chloride
- Product NDC
- 70518-2710
- 11-digit product format
- 705182710
- Labeler code
- 70518
- Product ID
- 70518-2710_d6e6445d-be8f-6894-e053-2995a90a8314
- 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
- 2020-04-24
- Marketing end
- 0000-00-00
- Substance
- OXYBUTYNIN CHLORIDE
- Active strength
- 15 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2710-0 | 70518271000 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2710-0) | 2020-04-24 | 0000-00-00 | No | No | Current |