leader loperamide
- Product NDC
- 49781-089
- 11-digit product format
- 497810089
- Labeler code
- 49781
- Product ID
- 49781-089_0beba1ac-7c94-4e36-ad14-08a5933a6f2c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loperamide Hydrochloride
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA091292
- Marketing category
- ANDA
- Marketing start
- 2014-05-30
- Marketing end
- 2020-03-01
- Substance
- LOPERAMIDE HYDROCHLORIDE
- Active strength
- 1 mg/7.5mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record