Dicyclomine Hydrochloride
- Product NDC
- 68071-1908
- 11-digit product format
- 680711908
- Labeler code
- 68071
- Product ID
- 68071-1908_49869e32-8eb0-5e29-e054-00144ff8d46c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA085223
- Marketing category
- ANDA
- Marketing start
- 1986-07-30
- 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