Oxybutynin Chloride
- Product NDC
- 70518-1941
- 11-digit product format
- 705181941
- Labeler code
- 70518
- Product ID
- 70518-1941_da6c2802-5d17-dbcb-e053-2a95a90a2561
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxybutynin Chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA209823
- Marketing category
- ANDA
- Marketing start
- 2019-03-08
- 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 |
|---|
| 70518-1941-0 | 70518194100 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-1941-0) | 90 tablet | 2019-03-08 | 0000-00-00 | No | No | Current |
| 70518-1941-1 | 70518194101 | 30 TABLET in 1 BLISTER PACK (70518-1941-1) | 30 tablet | 2019-03-29 | 0000-00-00 | No | No | Current |
| 70518-1941-2 | 70518194102 | 180 TABLET in 1 BOTTLE, PLASTIC (70518-1941-2) | 180 tablet | 2019-05-17 | 0000-00-00 | No | No | Current |
| 70518-1941-3 | 70518194103 | 60 TABLET in 1 BOTTLE, PLASTIC (70518-1941-3) | 60 tablet | 2019-07-14 | 0000-00-00 | No | No | Current |