Loperamide Hydrochloride
- Product NDC
- 42708-074
- 11-digit product format
- 427080074
- Labeler code
- 42708
- Product ID
- 42708-074_bbb5955b-f7c2-3602-e053-2a95a90a76a4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Loperamide Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- QPharma Inc
- Application
- ANDA073192
- Marketing category
- ANDA
- Marketing start
- 1993-05-01
- Marketing end
- 0000-00-00
- Substance
- LOPERAMIDE HYDROCHLORIDE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Opioid Agonist [EPC],Opioid Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 42708-074-24 | 42708007424 | 24 CAPSULE in 1 BOTTLE (42708-074-24) | 24 capsule | 2018-09-26 | 0000-00-00 | Yes | No | Current |