Dicyclomine Hydrochloride
- Product NDC
- 66267-074
- 11-digit product format
- 662670074
- Labeler code
- 66267
- Product ID
- 66267-074_9cbe92d6-d1f9-549c-e053-2995a90a1d8b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA040230
- Marketing category
- ANDA
- Marketing start
- 1999-02-26
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record