Dicyclomine Hydrochloride
- Product NDC
- 68788-6404
- 11-digit product format
- 687886404
- Labeler code
- 68788
- Product ID
- 68788-6404_595f786c-7d2e-4bb5-a0af-9dc306188124
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA040230
- Marketing category
- ANDA
- Marketing start
- 2016-06-09
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record