diethylpropion hydrochloride

Generic: diethylpropion hydrochloride

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

diethylpropion hydrochloride 25 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-348
Product ID 43063-348_41379e71-36e8-db5a-e063-6394a90a63ae
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 43063348
Hyphenated Format 43063-348

Supplemental Identifiers

RxCUI
978654
UPC
0343063348604
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
  • 100 TABLET in 1 BOTTLE, PLASTIC (43063-348-01)
  • 7 TABLET in 1 BOTTLE, PLASTIC (43063-348-07)
  • 14 TABLET in 1 BOTTLE, PLASTIC (43063-348-14)
  • 21 TABLET in 1 BOTTLE, PLASTIC (43063-348-21)
  • 28 TABLET in 1 BOTTLE, PLASTIC (43063-348-28)
  • 30 TABLET in 1 BOTTLE, PLASTIC (43063-348-30)
  • 56 TABLET in 1 BOTTLE, PLASTIC (43063-348-56)
  • 60 TABLET in 1 BOTTLE, PLASTIC (43063-348-60)
  • 90 TABLET in 1 BOTTLE, PLASTIC (43063-348-90)
  • 180 TABLET in 1 BOTTLE, PLASTIC (43063-348-93)
source: ndc

Packages (10)

Ingredients (1)

diethylpropion hydrochloride (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41379e71-36e8-db5a-e063-6394a90a63ae", "openfda": {"upc": ["0343063348604"], "unii": ["19V2PL39NG"], "rxcui": ["978654"], "spl_set_id": ["ad0c3dc9-ae13-4853-bc8c-a66e2a69cc10"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (43063-348-01)", "package_ndc": "43063-348-01", "marketing_start_date": "20120307"}, {"sample": false, "description": "7 TABLET in 1 BOTTLE, PLASTIC (43063-348-07)", "package_ndc": "43063-348-07", "marketing_start_date": "20120307"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (43063-348-14)", "package_ndc": "43063-348-14", "marketing_start_date": "20120307"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE, PLASTIC (43063-348-21)", "package_ndc": "43063-348-21", "marketing_start_date": "20120307"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE, PLASTIC (43063-348-28)", "package_ndc": "43063-348-28", "marketing_start_date": "20120307"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-348-30)", "package_ndc": "43063-348-30", "marketing_start_date": "20120307"}, {"sample": false, "description": "56 TABLET in 1 BOTTLE, PLASTIC (43063-348-56)", "package_ndc": "43063-348-56", "marketing_start_date": "20120307"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (43063-348-60)", "package_ndc": "43063-348-60", "marketing_start_date": "20120307"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-348-90)", "package_ndc": "43063-348-90", "marketing_start_date": "20120307"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE, PLASTIC (43063-348-93)", "package_ndc": "43063-348-93", "marketing_start_date": "20120307"}], "brand_name": "DIETHYLPROPION HYDROCHLORIDE", "product_id": "43063-348_41379e71-36e8-db5a-e063-6394a90a63ae", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "43063-348", "dea_schedule": "CIV", "generic_name": "DIETHYLPROPION HYDROCHLORIDE", "labeler_name": "PD-Rx 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"}