Loperamide Hydrochloride
- Product NDC
- 63629-8193
- 11-digit product format
- 636298193
- Labeler code
- 63629
- Product ID
- 63629-8193_eb2141cc-1547-4c77-be42-a7e8a730a538
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Loperamide Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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
- 2020-12-31
- 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 |
|---|
| 63629-8193-1 | 63629819301 | 15 CAPSULE in 1 BOTTLE (63629-8193-1) | 15 capsule | 2019-07-25 | 0000-00-00 | No | No | Current |