Bethanechol Chloride
- Product NDC
- 51293-647
- 11-digit product format
- 512930647
- Labeler code
- 51293
- Product ID
- 51293-647_a09fcea1-a58d-4333-a3cb-56766a74cac2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bethanechol Chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ECI Pharmaceuticals LLC
- Application
- ANDA040728
- Marketing category
- ANDA
- Marketing start
- 2020-02-15
- Marketing end
- 0000-00-00
- Substance
- BETHANECHOL CHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Cholinergic Muscarinic Agonist [EPC],Cholinergic Muscarinic Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51293-647 | BETHANECHOL CHLORIDE TABLET [ECI PHARMACEUTICALS LLC ] | 1 | Legacy NDC | 20200302_1cf5ba26-17a3-4adc-8990-4853a4177c1e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51293-647-01 | 51293064701 | 100 TABLET in 1 BOTTLE (51293-647-01) | 100 tablet | 2020-02-15 | 0000-00-00 | No | No | Current |