Dicyclomine hydrochloride
- Product NDC
- 70518-1732
- 11-digit product format
- 705181732
- Labeler code
- 70518
- Product ID
- 70518-1732_9631da54-17fe-a060-e053-2a95a90a91a6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040204
- Marketing category
- ANDA
- Marketing start
- 2018-12-14
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record