Package 68094-129-62
Brand: loperamide hydrochloride
Generic: loperamide hydrochloridePackage Facts
Identity
Package NDC
68094-129-62
Digits Only
6809412962
Product NDC
68094-129
Description
3 TRAY in 1 CASE (68094-129-62) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (68094-129-59)
Marketing
Marketing Status
Brand
loperamide hydrochloride
Generic
loperamide hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "73a0214b-3f58-4357-ab53-314111602166", "openfda": {"unii": ["77TI35393C"], "rxcui": ["1250685"], "spl_set_id": ["ae8237f0-95a6-4163-b476-25c0509ef151"], "manufacturer_name": ["Precision Dose, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "3 TRAY in 1 CASE (68094-129-62) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (68094-129-59)", "package_ndc": "68094-129-62", "marketing_start_date": "20200518"}], "brand_name": "Loperamide Hydrochloride", "product_id": "68094-129_73a0214b-3f58-4357-ab53-314111602166", "dosage_form": "SOLUTION", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "68094-129", "generic_name": "Loperamide Hydrochloride", "labeler_name": "Precision Dose, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loperamide Hydrochloride", "active_ingredients": [{"name": "LOPERAMIDE HYDROCHLORIDE", "strength": "1 mg/7.5mL"}], "application_number": "ANDA091292", "marketing_category": "ANDA", "marketing_start_date": "20200518", "listing_expiration_date": "20261231"}