diethylpropion hydrochloride

Generic: diethylpropion hydrochloride

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diethylpropion hydrochloride
Generic Name diethylpropion hydrochloride
Labeler nucare pharmaceuticals,inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

diethylpropion hydrochloride 25 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-3400
Product ID 68071-3400_2d54077e-4c8e-aaae-e063-6394a90adb41
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
appetite suppression [pe] increased sympathetic activity [pe] sympathomimetic amine anorectic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713400
Hyphenated Format 68071-3400

Supplemental Identifiers

RxCUI
978654
UPC
0368071340037
UNII
19V2PL39NG

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 112 TABLET in 1 BOTTLE (68071-3400-0)
  • 21 TABLET in 1 BOTTLE (68071-3400-1)
  • 42 TABLET in 1 BOTTLE (68071-3400-2)
  • 30 TABLET in 1 BOTTLE (68071-3400-3)
  • 84 TABLET in 1 BOTTLE (68071-3400-4)
  • 56 TABLET in 1 BOTTLE (68071-3400-5)
  • 14 TABLET in 1 BOTTLE (68071-3400-7)
source: ndc

Packages (7)

68071-3400-0 112 TABLET in 1 BOTTLE (68071-3400-0) 68071-3400-1 21 TABLET in 1 BOTTLE (68071-3400-1) 68071-3400-2 42 TABLET in 1 BOTTLE (68071-3400-2) 68071-3400-3 30 TABLET in 1 BOTTLE (68071-3400-3) 68071-3400-4 84 TABLET in 1 BOTTLE (68071-3400-4) 68071-3400-5 56 TABLET in 1 BOTTLE (68071-3400-5) 68071-3400-7 14 TABLET in 1 BOTTLE (68071-3400-7)

Ingredients (1)

diethylpropion hydrochloride (25 mg/1)

Linked Drug Pages (1)

DIETHYLPROPION HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2d54077e-4c8e-aaae-e063-6394a90adb41", "openfda": {"upc": ["0368071340037"], "unii": ["19V2PL39NG"], "rxcui": ["978654"], "spl_set_id": ["fe7e5022-8b58-aa4f-e053-6294a90af65e"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "112 TABLET in 1 BOTTLE (68071-3400-0)", "package_ndc": "68071-3400-0", "marketing_start_date": "20230619"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (68071-3400-1)", "package_ndc": "68071-3400-1", "marketing_start_date": "20230619"}, {"sample": false, "description": "42 TABLET in 1 BOTTLE (68071-3400-2)", "package_ndc": "68071-3400-2", "marketing_start_date": "20230619"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3400-3)", "package_ndc": "68071-3400-3", "marketing_start_date": "20230619"}, {"sample": false, "description": "84 TABLET in 1 BOTTLE (68071-3400-4)", "package_ndc": "68071-3400-4", "marketing_start_date": "20230619"}, {"sample": false, "description": "56 TABLET in 1 BOTTLE (68071-3400-5)", "package_ndc": "68071-3400-5", "marketing_start_date": "20230619"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (68071-3400-7)", "package_ndc": "68071-3400-7", "marketing_start_date": "20230619"}], "brand_name": "DIETHYLPROPION HYDROCHLORIDE", "product_id": "68071-3400_2d54077e-4c8e-aaae-e063-6394a90adb41", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "68071-3400", "dea_schedule": "CIV", "generic_name": "DIETHYLPROPION HYDROCHLORIDE", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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"}