Anti-Diarrheal
- Product NDC
- 50804-520
- 11-digit product format
- 508040520
- Labeler code
- 50804
- Product ID
- 50804-520_61ec15ff-c84a-4759-9076-1d0ad82410a6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- LOPERAMIDE HYDROCHLORIDE
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Good Sense (Geiss, Destin & Dunn, Inc.)
- Application
- NDA021855
- Marketing category
- NDA
- Marketing start
- 2010-07-15
- Marketing end
- 0000-00-00
- Substance
- LOPERAMIDE HYDROCHLORIDE
- Active strength
- 2 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50804-520-12 | 50804052012 | 1 BLISTER PACK in 1 BOX (50804-520-12) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK | 1 blister pack | 2010-07-15 | 0000-00-00 | No | No | Current |