Loperamide Hydrochloride
- Product NDC
- 58602-827
- 11-digit product format
- 586020827
- Labeler code
- 58602
- Product ID
- 58602-827_3691129b-7b06-4cd2-8652-dfd0c5443f0f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loperamide Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aurohealth LLC
- Application
- ANDA206548
- Marketing category
- ANDA
- Marketing start
- 2015-12-15
- Marketing end
- 0000-00-00
- Substance
- LOPERAMIDE HYDROCHLORIDE
- Active strength
- 2 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record