Dicyclomine hydrochloride
- Product NDC
- 50090-4681
- 11-digit product format
- 500904681
- Labeler code
- 50090
- Product ID
- 50090-4681_6b45be3a-4645-4191-bc72-ab797b2f95ef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040204
- Marketing category
- ANDA
- Marketing start
- 1997-02-28
- Marketing end
- 0000-00-00
- Substance
- DICYCLOMINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Anticholinergic [EPC],Cholinergic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 50090-4681-1 | 50090468101 | 28 CAPSULE in 1 BOTTLE (50090-4681-1) | 28 capsule | 2019-11-04 | 0000-00-00 | No | No | Current |