Phendimetrazine Tartrate

Product NDC
17224-800
11-digit product format
172240800
Labeler code
17224
Product ID
17224-800_2efc9fe0-08c0-3c64-e063-6294a90a6b4c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
PHENDIMETRAZINE TARTRATE
Dosage form
TABLET
Route
ORAL
Labeler
Calvin Scott & Co., Inc.
Application
ANDA091042
Marketing category
ANDA
Marketing start
1978-01-01
Substance
PHENDIMETRAZINE TARTRATE
Active strength
35 mg/1
Pharmacologic classes
Appetite Suppression [PE], Increased Sympathetic Activity [PE], Sympathomimetic Amine Anorectic [EPC]
DEA schedule
CIII
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Orange Book products#

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A091042-001PHENDIMETRAZINE TARTRATEPHENDIMETRAZINE TARTRATE35MGTABLET / ORALAA2010-08-31

Therapeutic equivalence codes#

Application-product, TE code table
Application-productTE code
A091042-001AA

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Phendimetrazine TartratePHENDIMETRAZINE TARTRATECalvin Scott & Co., Inc.f5c30a88-5814-5b42-e053-2995a90a437a2026-05-21Warnings, Adverse reactionsExact identifier

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

warnings

WARNINGS: Phendimetrazine tartrate should not be used in combination with other anorectic agents, including prescribed drugs, over-the-counter preparations and herbal products. In a case-control epidemiological study, the use of anorectic agents, including phendimetrazine tartrate, was associated with an increased risk of developing pulmonary hypertension, a rare, but often fatal disorder. The use of anorectic agents for longer than three months was associated with a 23-fold increase in the risk of developing pulmonary hypertension. Increased risk of pulmonary hypertension with repeated courses of therapy cannot be excluded. The onset or aggravation of exertional dyspnea, or unexplained symptoms of angina pectoris, syncope, or lower extremity edema suggest the possibility of occurrence of pulmonary hypertension. Under these circumstances, phendimetrazine tartrate should be immediately discontinued, and the patient should be evaluated for the possible presence of pulmonary hypertension. Valvular heart disease associated with the use of some anorectic agents such as fenfluramine and dexfenfluramine has been reported. Possible contributing factors include use for extended periods of time, higher than recommended dose, and/or use in combination with other anorectic drugs. However, no cases of this valvulopathy have been reported when phendimetrazine tartrate has been used alone. The potential risk of possible serious adverse effects such as valvular heart disease and pulmonary hypertension should be assessed carefully against the potential benefit of weight loss. Baseline cardiac evaluation should be considered to detect pre-existing valvular heart diseases or pulmonary hypertension prior to initiation of phendimetrazine treatment. Phendimetrazine tartrate is not recommended in patients with known heart murmur or valvular heart disease. Echocardiogram during and after treatment could be useful for detecting any valvular disorders which may occur. To limit unwarranted exposure and risks, treatment with phendimetrazine tartrate should be continued only if the patient has satisfactory weight loss within the first 4 weeks of treatment (i.e., weight loss of at least 4 pounds, or as determined by the physician and patient). Tolerance to the anorectic effect of phendimetrazine develops within a few weeks. When this occurs, its use should be discontinued; the maximum...

Adverse reactions cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

adverse reactions

ADVERSE REACTIONS: Cardiovascular: Palpitations, tachycardia, elevated blood pressure, ischemic events. Valvular heart disease associated with the use of some anorectic agents such as fenfluramine and dexfenfluramine, both independently and especially when used in combination with other anorectic drugs, have been reported. However, no case of this valvulopathy has been reported when phendimetrazine tartrate has been used alone. Central Nervous System: Overstimulation, restlessness, insomnia, agitation, flushing, tremor, sweating, dizziness, headache, psychotic state, blurring of vision. Gastrointestinal: Dryness of the mouth, nausea, diarrhea, constipation, stomach pain. Genitourinary: Urinary frequency, dysuria, changes in libido.

Additional Listing Data#

Finished product
Yes
Brand name base
Phendimetrazine Tartrate
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PHENDIMETRAZINE TARTRATE35 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii6985IP0T80
Rxcui979549

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
71525015-bcb9-5864-7749-4b5f528a6b6aProduct name220180419
977c925f-5460-67b1-e843-25a0ba370df1Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17224-800-14Phendimetrazine Tartrate14 in 1 BOTTLE, PLASTICTABLET142
17224-800-18Phendimetrazine Tartrate180 in 1 BOTTLE, PLASTICTABLET1802
17224-800-28Phendimetrazine Tartrate28 in 1 BOTTLE, PLASTICTABLET282
17224-800-30Phendimetrazine Tartrate30 in 1 BOTTLE, PLASTICTABLET302
17224-800-42Phendimetrazine Tartrate42 in 1 BOTTLE, PLASTICTABLET422
17224-800-56Phendimetrazine Tartrate56 in 1 BOTTLE, PLASTICTABLET562
17224-800-60Phendimetrazine Tartrate60 in 1 BOTTLE, PLASTICTABLET602
17224-800-68Phendimetrazine Tartrate168 in 1 BOTTLE, PLASTICTABLET1682
17224-800-84Phendimetrazine Tartrate84 in 1 BOTTLE, PLASTICTABLET842
17224-800-90Phendimetrazine Tartrate90 in 1 BOTTLE, PLASTICTABLET902

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17224-800PHENDIMETRAZINE TARTRATE TABLET [CALVIN SCOTT & CO., INC.]2Current NDC, 10 package rows20250227_f5c30a88-5814-5b42-e053-2995a90a437a.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
979549phendimetrazine tartrate 35 MG Oral TabletPSNf5c30a88-5814-5b42-e053-2995a90a437a3
979549phendimetrazine tartrate 35 MG Oral TabletSCDf5c30a88-5814-5b42-e053-2995a90a437a3

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
17224-800-141722408001414 TABLET in 1 BOTTLE, PLASTIC (17224-800-14) 14 tablet1978-01-01NoNoCurrent
17224-800-1817224080018180 TABLET in 1 BOTTLE, PLASTIC (17224-800-18) 180 tablet1978-01-01NoNoCurrent
17224-800-281722408002828 TABLET in 1 BOTTLE, PLASTIC (17224-800-28) 28 tablet1978-01-01NoNoCurrent
17224-800-301722408003030 TABLET in 1 BOTTLE, PLASTIC (17224-800-30) 30 tablet1978-01-01NoNoCurrent
17224-800-421722408004242 TABLET in 1 BOTTLE, PLASTIC (17224-800-42) 42 tablet1978-01-01NoNoCurrent
17224-800-561722408005656 TABLET in 1 BOTTLE, PLASTIC (17224-800-56) 56 tablet1978-01-01NoNoCurrent
17224-800-601722408006060 TABLET in 1 BOTTLE, PLASTIC (17224-800-60) 60 tablet1978-01-01NoNoCurrent
17224-800-631722408006363 TABLET in 1 BOTTLE, PLASTIC (17224-800-63)63 tablet1978-01-010Current
17224-800-6817224080068168 TABLET in 1 BOTTLE, PLASTIC (17224-800-68) 168 tablet1978-01-01NoNoCurrent
17224-800-841722408008484 TABLET in 1 BOTTLE, PLASTIC (17224-800-84) 84 tablet1978-01-01NoNoCurrent
17224-800-901722408009090 TABLET in 1 BOTTLE, PLASTIC (17224-800-90) 90 tablet1978-01-01NoNoCurrent