Package 42291-067-30

Brand: atomoxetine

Generic: atomoxetine
NDC Package

Package Facts

Identity

Package NDC 42291-067-30
Digits Only 4229106730
Product NDC 42291-067
Description

30 CAPSULE in 1 BOTTLE (42291-067-30)

Marketing

Marketing Status
Marketed Since 2022-04-12
Brand atomoxetine
Generic atomoxetine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "485b5018-57ec-90d7-e063-6294a90ae5e2", "openfda": {"upc": ["0342291066304", "0342291069305", "0342291068308", "0342291064300", "0342291070301", "0342291067301"], "unii": ["57WVB6I2W0"], "rxcui": ["349591", "349592", "349593", "349594", "349595", "608139", "608143"], "spl_set_id": ["dc7ba02c-bdbb-5136-e053-2995a90ac545"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (42291-067-30)", "package_ndc": "42291-067-30", "marketing_start_date": "20220412"}], "brand_name": "Atomoxetine", "product_id": "42291-067_485b5018-57ec-90d7-e063-6294a90ae5e2", "dosage_form": "CAPSULE", "pharm_class": ["Norepinephrine Reuptake Inhibitor [EPC]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "42291-067", "generic_name": "Atomoxetine", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atomoxetine", "active_ingredients": [{"name": "ATOMOXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA079022", "marketing_category": "ANDA", "marketing_start_date": "20220412", "listing_expiration_date": "20271231"}