Dicyclomine Hydrochloride
- Product NDC
- 55154-5684
- 11-digit product format
- 551545684
- Labeler code
- 55154
- Product ID
- 55154-5684_216431a6-cd42-45f7-96c3-8f32fcbab33f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA040317
- Marketing category
- ANDA
- Marketing start
- 2011-08-16
- 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