OXYBUTYNIN CHLORIDE
- Product NDC
- 70518-3473
- 11-digit product format
- 705183473
- Labeler code
- 70518
- Product ID
- 70518-3473_e5e49d98-7965-867e-e053-2a95a90a0862
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- OXYBUTYNIN CHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA212798
- Marketing category
- ANDA
- Marketing start
- 2022-08-09
- 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
- 2023-12-31
- 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 |
|---|
| 70518-3473-0 | 70518347300 | 30 TABLET in 1 BLISTER PACK (70518-3473-0) | 30 tablet | 2022-08-09 | 0000-00-00 | No | No | Current |