Urecholine
- Product NDC
- 51285-692
- 11-digit product format
- 512850692
- Labeler code
- 51285
- Product ID
- 51285-692_c08ddeaf-c772-4e32-92a8-9fb81dc94ddb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bethanechol Chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Teva Women's Health, Inc.
- Application
- ANDA089096
- Marketing category
- ANDA
- Marketing start
- 2001-02-01
- Marketing end
- 2021-02-28
- 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 |
|---|
| 51285-692-02 | 51285069202 | 100 TABLET in 1 BOTTLE (51285-692-02) | 100 tablet | 2001-02-01 | 2021-02-28 | No | No | Current |