Dicyclomine Hydrochloride
- Product NDC
- 51079-119
- 11-digit product format
- 510790119
- Labeler code
- 51079
- Product ID
- 51079-119_9e02e57e-46d2-88ea-e053-2995a90a573e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dicyclomine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA040317
- Marketing category
- ANDA
- Marketing start
- 1998-03-06
- Marketing end
- 2020-11-30
- Substance
- DICYCLOMINE HYDROCHLORIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Anticholinergic [EPC],Cholinergic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record