Dicyclomine Hydrochloride
- Product NDC
- 50090-2863
- 11-digit product format
- 500902863
- Labeler code
- 50090
- Product ID
- 50090-2863_68918e38-21b6-4668-86e0-a1b01c9838ba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#