Loperamide Hydrochloride
- Product NDC
- 71335-2111
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Loperamide Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA215001
- Marketing category
- ANDA
- Substance
- LOPERAMIDE HYDROCHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 71335-2111-4 | 12 CAPSULE in 1 BOTTLE (71335-2111-4) | 20220620 | No | Historical |
Related DailyMed Labels
| Set ID | Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|---|
| 1e9dfe71-28a9-4b54-a0e1-7c0d82fec0d7 | Loperamide Hydrochloride | Bryant Ranch Prepack | 2023-05-24 | HUMAN PRESCRIPTION DRUG LABEL | 101 |