Dicyclomine Hydrochloride
- Product NDC
- 60760-795
- 11-digit product format
- 607600795
- Labeler code
- 60760
- Product ID
- 60760-795_77e497c0-97a1-cc9b-e053-2991aa0a57d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA085223
- Marketing category
- ANDA
- Marketing start
- 1986-07-30
- Marketing end
- 2019-06-30
- Substance
- DICYCLOMINE HYDROCHLORIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Anticholinergic [EPC],Cholinergic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record