Loperamide Hydrochloride
- Product NDC
- 43063-431
- 11-digit product format
- 430630431
- Labeler code
- 43063
- Product ID
- 43063-431_7c4a36ea-6ddb-51a2-e053-2a91aa0acf37
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- loperamide hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA072741
- Marketing category
- ANDA
- Marketing start
- 1991-09-18
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record