Dicyclomine Hydrochloride
- Product NDC
- 55700-359
- 11-digit product format
- 557000359
- Labeler code
- 55700
- Product ID
- 55700-359_b8915518-54aa-4f05-86ed-50b1379958f7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dicyclomine hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA040319
- Marketing category
- ANDA
- Marketing start
- 2016-01-22
- 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