Package 60505-2831-3
Brand: atomoxetine hydrochloride
Generic: atomoxetine hydrochloridePackage Facts
Identity
Package NDC
60505-2831-3
Digits Only
6050528313
Product NDC
60505-2831
Description
30 CAPSULE in 1 BOTTLE (60505-2831-3)
Marketing
Marketing Status
Brand
atomoxetine hydrochloride
Generic
atomoxetine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ad1d5a70-74b7-c5db-b589-88081ba704f9", "openfda": {"unii": ["57WVB6I2W0"], "rxcui": ["349591", "349592", "349593", "349594", "349595", "608139", "608143"], "spl_set_id": ["132852a6-5bff-15dd-255c-98309dd83630"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (60505-2831-3)", "package_ndc": "60505-2831-3", "marketing_start_date": "20180521"}], "brand_name": "Atomoxetine Hydrochloride", "product_id": "60505-2831_ad1d5a70-74b7-c5db-b589-88081ba704f9", "dosage_form": "CAPSULE", "pharm_class": ["Norepinephrine Reuptake Inhibitor [EPC]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "60505-2831", "generic_name": "atomoxetine hydrochloride", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atomoxetine Hydrochloride", "active_ingredients": [{"name": "ATOMOXETINE HYDROCHLORIDE", "strength": "18 mg/1"}], "application_number": "ANDA078983", "marketing_category": "ANDA", "marketing_start_date": "20180521", "listing_expiration_date": "20261231"}