Package 43063-532-30

Brand: diethylpropion hydrochloride er

Generic: diethylpropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43063-532-30
Digits Only 4306353230
Product NDC 43063-532
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-532-30)

Marketing

Marketing Status
Marketed Since 2014-07-25
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": "413931e3-aacb-4898-e063-6294a90a5b6b", "openfda": {"upc": ["0343063532072"], "unii": ["19V2PL39NG"], "rxcui": ["978668"], "spl_set_id": ["0d213a24-ebbf-41df-8f32-de44a572829e"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-532-07)", "package_ndc": "43063-532-07", "marketing_start_date": "20140630"}, {"sample": false, "description": "14 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-532-14)", "package_ndc": "43063-532-14", "marketing_start_date": "20140630"}, {"sample": false, "description": "21 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-532-21)", "package_ndc": "43063-532-21", "marketing_start_date": "20171219"}, {"sample": false, "description": "28 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-532-28)", "package_ndc": "43063-532-28", "marketing_start_date": "20161114"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-532-30)", "package_ndc": "43063-532-30", "marketing_start_date": "20140725"}], "brand_name": "Diethylpropion Hydrochloride ER", "product_id": "43063-532_413931e3-aacb-4898-e063-6294a90a5b6b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "43063-532", "dea_schedule": "CIV", "generic_name": "Diethylpropion Hydrochloride", "labeler_name": "PD-Rx 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"}