Bethanechol Chloride
- Product NDC
- 71335-0846
- 11-digit product format
- 713350846
- Labeler code
- 71335
- Product ID
- 71335-0846_76a04f69-f035-441e-b62c-3fd3c1a40c61
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bethanechol Chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040855
- Marketing category
- ANDA
- Marketing start
- 2007-11-21
- Marketing end
- 0000-00-00
- Substance
- BETHANECHOL CHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Cholinergic Muscarinic Agonist [EPC], Cholinergic Muscarinic Agonists [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 |
|---|
| 71335-0846-1 | 71335084601 | 30 TABLET in 1 BOTTLE (71335-0846-1) | 30 tablet | 2018-05-31 | 0000-00-00 | No | No | Current |
| 71335-0846-2 | 71335084602 | 28 TABLET in 1 BOTTLE (71335-0846-2) | 28 tablet | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0846-3 | 71335084603 | 90 TABLET in 1 BOTTLE (71335-0846-3) | 90 tablet | 2021-12-27 | 0000-00-00 | No | No | Current |