Dicyclomine hydrochloride
- Product NDC
- 50090-4677
- 11-digit product format
- 500904677
- Labeler code
- 50090
- Product ID
- 50090-4677_028267dd-3b78-459c-b938-6489ae6f90f4
- 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 |
|---|
| 50090-4677-0 | 50090467700 | 30 CAPSULE in 1 BOTTLE (50090-4677-0) | 30 capsule | 2019-11-04 | 0000-00-00 | No | No | Current |
| 50090-4677-2 | 50090467702 | 60 CAPSULE in 1 BOTTLE (50090-4677-2) | 60 capsule | 2019-11-04 | 0000-00-00 | No | No | Current |
| 50090-4677-8 | 50090467708 | 90 CAPSULE in 1 BOTTLE (50090-4677-8) | 90 capsule | 2019-11-04 | 0000-00-00 | No | No | Current |