Bethanechol Chloride
- Product NDC
- 50111-326
- 11-digit product format
- 501110326
- Labeler code
- 50111
- Product ID
- 50111-326_c4ba78e1-9856-48c3-8bc2-643a96e33c89
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bethanechol Chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA089096
- Marketing category
- ANDA
- Marketing start
- 1990-09-30
- Marketing end
- 2021-03-31
- Substance
- BETHANECHOL CHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Cholinergic Muscarinic Agonist [EPC],Cholinergic Muscarinic Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 50111-326-01 | 50111032601 | 100 TABLET in 1 BOTTLE (50111-326-01) | 100 tablet | 1990-09-30 | 2021-03-31 | No | No | Current |