Dicyclomine Hydrochloride
- Product NDC
- 71610-118
- 11-digit product format
- 716100118
- Labeler code
- 71610
- Product ID
- 71610-118_80229afc-b532-43b4-8955-9efc27a74a4e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dicyclomine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- 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
- 2020-12-31
- 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 |
|---|
| 71610-118-09 | 71610011809 | 9000 TABLET in 1 BOTTLE, PLASTIC (71610-118-09) | 9000 tablet | 2018-08-15 | 0000-00-00 | No | No | Current |