dicyclomine hydrochloride
- Product NDC
- 46672-657
- 11-digit product format
- 466720657
- Labeler code
- 46672
- Product ID
- 46672-657_3fdc101a-6deb-481f-ac50-de4aa9198142
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dicyclomine hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Mikart, Inc.
- Application
- ANDA040169
- Marketing category
- ANDA
- Marketing start
- 2005-03-24
- Marketing end
- 0000-00-00
- Substance
- DICYCLOMINE HYDROCHLORIDE
- Active strength
- 10 mg/5mL
- Pharmacologic classes
- Anticholinergic [EPC],Cholinergic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record