Oxybutynin Chloride
- Product NDC
- 70518-2904
- 11-digit product format
- 705182904
- Labeler code
- 70518
- Product ID
- 70518-2904_d79738eb-a047-662a-e053-2995a90abdf1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxybutynin Chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA211682
- Marketing category
- ANDA
- Marketing start
- 2020-10-08
- 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
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 |
|---|
| 70518-2904-0 | 70518290400 | 30 TABLET in 1 BLISTER PACK (70518-2904-0) | 30 tablet | 2020-10-08 | 0000-00-00 | No | No | Current |
| 70518-2904-1 | 70518290401 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-2904-1) | 90 tablet | 2020-11-13 | 0000-00-00 | No | No | Current |