Dicyclomine
- Product NDC
- 0615-1516
- 11-digit product format
- 006151516
- Labeler code
- 0615
- Product ID
- 0615-1516_c966c621-8959-467b-8abb-3149912e410c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA040161
- Marketing category
- ANDA
- Marketing start
- 1996-10-01
- 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