phentermine hydrochloride

Generic: phentermine hydrochloride

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

Drug Facts

Product Profile

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

phentermine hydrochloride 30 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-470
Product ID 72789-470_2eea1bf6-c5c0-5da8-e063-6394a90a792c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202248
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2024-02-15

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 72789470
Hyphenated Format 72789-470

Supplemental Identifiers

RxCUI
900038
UPC
0372789470078
UNII
0K2I505OTV

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 phentermine hydrochloride (source: ndc)
Generic Name phentermine hydrochloride (source: ndc)
Application Number ANDA202248 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 7 CAPSULE in 1 BOTTLE, PLASTIC (72789-470-07)
  • 14 CAPSULE in 1 BOTTLE, PLASTIC (72789-470-14)
  • 21 CAPSULE in 1 BOTTLE, PLASTIC (72789-470-21)
  • 30 CAPSULE in 1 BOTTLE, PLASTIC (72789-470-30)
source: ndc

Packages (4)

72789-470-07 7 CAPSULE in 1 BOTTLE, PLASTIC (72789-470-07) 72789-470-14 14 CAPSULE in 1 BOTTLE, PLASTIC (72789-470-14) 72789-470-21 21 CAPSULE in 1 BOTTLE, PLASTIC (72789-470-21) 72789-470-30 30 CAPSULE in 1 BOTTLE, PLASTIC (72789-470-30)

Ingredients (1)

phentermine hydrochloride (30 mg/1)

Linked Drug Pages (1)

Phentermine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2eea1bf6-c5c0-5da8-e063-6394a90a792c", "openfda": {"upc": ["0372789470078"], "unii": ["0K2I505OTV"], "rxcui": ["900038"], "spl_set_id": ["b425840f-380e-42bd-852a-6ee3641977ce"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "7 CAPSULE in 1 BOTTLE, PLASTIC (72789-470-07)", "package_ndc": "72789-470-07", "marketing_start_date": "20250113"}, {"sample": false, "description": "14 CAPSULE in 1 BOTTLE, PLASTIC (72789-470-14)", "package_ndc": "72789-470-14", "marketing_start_date": "20250210"}, {"sample": false, "description": "21 CAPSULE in 1 BOTTLE, PLASTIC (72789-470-21)", "package_ndc": "72789-470-21", "marketing_start_date": "20250205"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (72789-470-30)", "package_ndc": "72789-470-30", "marketing_start_date": "20250224"}], "brand_name": "Phentermine Hydrochloride", "product_id": "72789-470_2eea1bf6-c5c0-5da8-e063-6394a90a792c", "dosage_form": "CAPSULE", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "72789-470", "dea_schedule": "CIV", "generic_name": "Phentermine Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phentermine Hydrochloride", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA202248", "marketing_category": "ANDA", "marketing_start_date": "20240215", "listing_expiration_date": "20261231"}