Loperamide Hydrochloride
- Product NDC
- 70518-0072
- 11-digit product format
- 705180072
- Labeler code
- 70518
- Product ID
- 70518-0072_e64ce2a5-a1f5-5b4a-e053-2995a90a076c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Loperamide Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA073192
- Marketing category
- ANDA
- Marketing start
- 2016-12-19
- 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
- 2023-12-31
- 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 |
|---|
| 70518-0072-2 | 70518007202 | 15 CAPSULE in 1 BLISTER PACK (70518-0072-2) | 15 capsule | 2022-04-05 | 0000-00-00 | No | No | Current |