oxybutynin chloride
- Product NDC
- 70518-2388
- 11-digit product format
- 705182388
- Labeler code
- 70518
- Product ID
- 70518-2388_db98778e-52f8-0b2f-e053-2a95a90ae069
- 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
- 2019-10-25
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2388-0 | 70518238800 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2388-0) | 2019-10-25 | 0000-00-00 | No | No | Current |
| 70518-2388-1 | 70518238801 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2388-1) | 2020-09-15 | 0000-00-00 | No | No | Current |