OXYBUTYNIN CHLORIDE
- Product NDC
- 68788-7234
- 11-digit product format
- 687887234
- Labeler code
- 68788
- Product ID
- 68788-7234_d4345524-bde2-4076-89ab-03c3c6768a95
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- OXYBUTYNIN CHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA209025
- Marketing category
- ANDA
- Marketing start
- 2018-08-07
- 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
- 2021-12-31
- 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 |
|---|
| 68788-7234-1 | 68788723401 | 100 TABLET in 1 BOTTLE (68788-7234-1) | 100 tablet | 2018-08-07 | 0000-00-00 | No | No | Current |
| 68788-7234-2 | 68788723402 | 20 TABLET in 1 BOTTLE (68788-7234-2) | 20 tablet | 2018-08-07 | 0000-00-00 | No | No | Current |
| 68788-7234-3 | 68788723403 | 30 TABLET in 1 BOTTLE (68788-7234-3) | 30 tablet | 2018-08-07 | 0000-00-00 | No | No | Current |
| 68788-7234-6 | 68788723406 | 60 TABLET in 1 BOTTLE (68788-7234-6) | 60 tablet | 2018-08-07 | 0000-00-00 | No | No | Current |
| 68788-7234-9 | 68788723409 | 90 TABLET in 1 BOTTLE (68788-7234-9) | 90 tablet | 2018-08-07 | 0000-00-00 | No | No | Current |