Loperamide Hydrochloride
- Product NDC
- 67091-239
- 11-digit product format
- 670910239
- Labeler code
- 67091
- Product ID
- 67091-239_358ee5fb-b915-47a8-9075-20d07f8f023b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loperamide Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- WinCo Foods, LLC
- Application
- ANDA074091
- Marketing category
- ANDA
- Marketing start
- 1993-02-01
- Marketing end
- 2021-12-31
- Substance
- LOPERAMIDE HYDROCHLORIDE
- Active strength
- 2 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67091-239-12 | 67091023912 | 60 TABLET in 1 CARTON (67091-239-12) | 60 tablet | 2015-01-08 | 2021-12-31 | No | No | Current |