phentermine hydrochloride

Generic: phentermine hydrochloride

Labeler: precision dose inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name phentermine hydrochloride
Generic Name phentermine hydrochloride
Labeler precision dose inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phentermine hydrochloride 37.5 mg/1

Manufacturer
Precision Dose Inc.

Identifiers & Regulatory

Product NDC 68094-702
Product ID 68094-702_f245e2f3-2d40-468d-85f2-2fd47d2883d1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200272
DEA Schedule civ
Marketing Start 2024-02-15
Marketing End 2028-04-30

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 68094702
Hyphenated Format 68094-702

Supplemental Identifiers

RxCUI
803353
UPC
0368094702706
UNII
0K2I505OTV

Packaging Origin

Original Packager
true

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 ANDA200272 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68094-702-50)
  • 1000 TABLET in 1 BOTTLE (68094-702-70)
source: ndc

Packages (2)

68094-702-50 100 TABLET in 1 BOTTLE (68094-702-50) 68094-702-70 1000 TABLET in 1 BOTTLE (68094-702-70)

Ingredients (1)

phentermine hydrochloride (37.5 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": "f245e2f3-2d40-468d-85f2-2fd47d2883d1", "openfda": {"upc": ["0368094702706"], "unii": ["0K2I505OTV"], "rxcui": ["803353"], "spl_set_id": ["8d5697b9-02e8-40c4-97c7-761d635243c8"], "manufacturer_name": ["Precision Dose Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68094-702-50)", "package_ndc": "68094-702-50", "marketing_end_date": "20280430", "marketing_start_date": "20240215"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (68094-702-70)", "package_ndc": "68094-702-70", "marketing_end_date": "20280430", "marketing_start_date": "20240215"}], "brand_name": "Phentermine Hydrochloride", "product_id": "68094-702_f245e2f3-2d40-468d-85f2-2fd47d2883d1", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "68094-702", "dea_schedule": "CIV", "generic_name": "Phentermine Hydrochloride", "labeler_name": "Precision Dose Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phentermine Hydrochloride", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA200272", "marketing_category": "ANDA", "marketing_end_date": "20280430", "marketing_start_date": "20240215"}