Dicyclomine Hydrochloride
- Product NDC
- 50090-2186
- 11-digit product format
- 500902186
- Labeler code
- 50090
- Product ID
- 50090-2186_4545691c-d4d2-4c5d-8701-0c8192ed4e35
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dicyclomine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040317
- Marketing category
- ANDA
- Marketing start
- 1999-11-03
- Marketing end
- 0000-00-00
- Substance
- DICYCLOMINE HYDROCHLORIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Anticholinergic [EPC],Cholinergic 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 |
|---|
| 50090-2186-2 | 50090218602 | 20 TABLET in 1 BOTTLE (50090-2186-2) | 20 tablet | 2015-10-26 | 0000-00-00 | No | No | Current |