Oxybutynin Chloride
- Product NDC
- 68788-7785
- 11-digit product format
- 687887785
- Labeler code
- 68788
- Product ID
- 68788-7785_94dddbf0-87cf-4b78-9a88-1584b6dbd860
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxybutynin Chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA211062
- Marketing category
- ANDA
- Marketing start
- 2020-10-20
- 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 |
|---|
| 68788-7785-1 | 68788778501 | 100 TABLET in 1 BOTTLE (68788-7785-1) | 100 tablet | 2020-10-20 | 0000-00-00 | No | No | Current |
| 68788-7785-2 | 68788778502 | 20 TABLET in 1 BOTTLE (68788-7785-2) | 20 tablet | 2020-10-20 | 0000-00-00 | No | No | Current |
| 68788-7785-3 | 68788778503 | 30 TABLET in 1 BOTTLE (68788-7785-3) | 30 tablet | 2020-10-20 | 0000-00-00 | No | No | Current |
| 68788-7785-6 | 68788778506 | 60 TABLET in 1 BOTTLE (68788-7785-6) | 60 tablet | 2020-10-20 | 0000-00-00 | No | No | Current |
| 68788-7785-9 | 68788778509 | 90 TABLET in 1 BOTTLE (68788-7785-9) | 90 tablet | 2020-10-20 | 0000-00-00 | No | No | Current |