TROSPIUM CHLORIDE
- Product NDC
- 42291-846
- 11-digit product format
- 422910846
- Labeler code
- 42291
- Product ID
- 42291-846_9c950e60-c85c-4d8f-e053-2995a90a1d90
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- TROSPIUM CHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA091513
- Marketing category
- ANDA
- Marketing start
- 2016-10-06
- Marketing end
- 0000-00-00
- Substance
- TROSPIUM CHLORIDE
- Active strength
- 20 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-846-60 | 42291084660 | 60 TABLET in 1 BOTTLE (42291-846-60) | 60 tablet | 2016-10-06 | 0000-00-00 | No | No | Current |