diethylpropion hydrochloride
Generic: diethylpropion hydrochloride
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
diethylpropion hydrochloride
Generic Name
diethylpropion hydrochloride
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
diethylpropion hydrochloride 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-0327
Product ID
50090-0327_cea24273-8f72-4e34-a942-0d967378b7df
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA201212
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
2010-12-27
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500900327
Hyphenated Format
50090-0327
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
diethylpropion hydrochloride (source: ndc)
Generic Name
diethylpropion hydrochloride (source: ndc)
Application Number
ANDA201212 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 45 TABLET in 1 BOTTLE (50090-0327-0)
- 14 TABLET in 1 BOTTLE (50090-0327-3)
- 28 TABLET in 1 BOTTLE (50090-0327-4)
- 90 TABLET in 1 BOTTLE (50090-0327-5)
- 60 TABLET in 1 BOTTLE (50090-0327-7)
- 30 TABLET in 1 BOTTLE (50090-0327-8)
Packages (6)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cea24273-8f72-4e34-a942-0d967378b7df", "openfda": {"unii": ["19V2PL39NG"], "rxcui": ["978654"], "spl_set_id": ["fca52c33-b2c9-46cb-affc-2d6d23730f37"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "45 TABLET in 1 BOTTLE (50090-0327-0)", "package_ndc": "50090-0327-0", "marketing_start_date": "20181101"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (50090-0327-3)", "package_ndc": "50090-0327-3", "marketing_start_date": "20141128"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (50090-0327-4)", "package_ndc": "50090-0327-4", "marketing_start_date": "20141128"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-0327-5)", "package_ndc": "50090-0327-5", "marketing_start_date": "20141128"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-0327-7)", "package_ndc": "50090-0327-7", "marketing_start_date": "20141128"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-0327-8)", "package_ndc": "50090-0327-8", "marketing_start_date": "20141128"}], "brand_name": "DIETHYLPROPION HYDROCHLORIDE", "product_id": "50090-0327_cea24273-8f72-4e34-a942-0d967378b7df", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "50090-0327", "dea_schedule": "CIV", "generic_name": "DIETHYLPROPION HYDROCHLORIDE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DIETHYLPROPION HYDROCHLORIDE", "active_ingredients": [{"name": "DIETHYLPROPION HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA201212", "marketing_category": "ANDA", "marketing_start_date": "20101227", "listing_expiration_date": "20261231"}