Dicyclomine Hydrochloride
- Product NDC
- 68788-9935
- 11-digit product format
- 687889935
- Labeler code
- 68788
- Product ID
- 68788-9935_1a7c040c-54ea-411b-92cf-09b0ee7e7771
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc
- Application
- ANDA040204
- Marketing category
- ANDA
- Marketing start
- 2012-01-17
- Marketing end
- 0000-00-00
- Substance
- DICYCLOMINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Anticholinergic [EPC],Cholinergic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record