Package 68071-3837-1

Brand: diethylpropion hydrochloride er

Generic: diethylpropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3837-1
Digits Only 6807138371
Product NDC 68071-3837
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3837-1)

Marketing

Marketing Status
Marketed Since 2025-04-21
Brand diethylpropion hydrochloride er
Generic diethylpropion hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "33525ede-2f09-2ead-e063-6394a90a9ef1", "openfda": {"upc": ["0368071383713"], "unii": ["19V2PL39NG"], "rxcui": ["978668"], "spl_set_id": ["335265e0-1d5d-31fb-e063-6394a90a2e75"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3837-1)", "package_ndc": "68071-3837-1", "marketing_start_date": "20250421"}], "brand_name": "Diethylpropion Hydrochloride ER", "product_id": "68071-3837_33525ede-2f09-2ead-e063-6394a90a9ef1", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "68071-3837", "dea_schedule": "CIV", "generic_name": "Diethylpropion Hydrochloride", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diethylpropion Hydrochloride", "brand_name_suffix": "ER", "active_ingredients": [{"name": "DIETHYLPROPION HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA091680", "marketing_category": "ANDA", "marketing_start_date": "20111024", "listing_expiration_date": "20261231"}