Phendimetrazine Tartrate

Product NDC
52959-282
11-digit product format
529590282
Labeler code
52959
Product ID
52959-282_76692cfd-6252-450d-e053-2a91aa0a742f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Phendimetrazine Tartrate
Dosage form
TABLET
Route
ORAL
Labeler
H.J. Harkins Company, Inc.
Application
ANDA091042
Marketing category
ANDA
Marketing start
2010-09-15
Marketing end
0000-00-00
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
2019-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct52959-282IInactivated by FDA2026-07-31
excluded packagepackage52959-28252959-282-07IInactivated by FDA2026-07-31
excluded packagepackage52959-28252959-282-14IInactivated by FDA2026-07-31
excluded packagepackage52959-28252959-282-21IInactivated by FDA2026-07-31
excluded packagepackage52959-28252959-282-28IInactivated by FDA2026-07-31
excluded packagepackage52959-28252959-282-30IInactivated by FDA2026-07-31
excluded packagepackage52959-28252959-282-35IInactivated by FDA2026-07-31
excluded packagepackage52959-28252959-282-42IInactivated by FDA2026-07-31
excluded packagepackage52959-28252959-282-60IInactivated by FDA2026-07-31
excluded packagepackage52959-28252959-282-90IInactivated by FDA2026-07-31

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
Phendimetrazine TartratePHENDIMETRAZINE TARTRATEA-S Medication Solutionsef4cfd54-7d3e-4571-ae77-38ab2fd1af3d2026-01-29Warnings, Adverse reactionsExact identifier
Phendimetrazine TartratePHENDIMETRAZINE TARTRATEPreferred Pharmaceuticals Inc.767b5386-1e56-4eeb-8d59-510b940ab75e2025-09-08Warnings, Adverse reactionsExact identifier
Phendimetrazine TartratePHENDIMETRAZINE TARTRATENuCare Pharmaceuticals, Inc.342bc2a2-2751-b51a-e063-6394a90a4c432025-05-02Warnings, Adverse reactionsExact identifier
Phendimetrazine TartratePHENDIMETRAZINE TARTRATEA-S Medication Solutionsf1d265e1-522e-4a62-afda-29477fb94b8d2025-04-04Warnings, Adverse reactionsExact identifier
Phendimetrazine TartratePHENDIMETRAZINE TARTRATEPD-Rx Pharmaceuticals, Inc.467ae7d7-e342-423b-be89-5d38c1abf3c92025-01-08Warnings, Adverse reactionsExact identifier
Phendimetrazine TartratePHENDIMETRAZINE TARTRATEKVK-TECH, INC07bf3488-09e7-436f-af3f-94c35a7be0252024-12-06Warnings, Adverse reactionsExact identifier
Phendimetrazine TartratePHENDIMETRAZINE TARTRATENuCare Pharmaceuticals, Inc,40e5b0bf-347e-30f6-e054-00144ff88e882024-08-14Warnings, Adverse reactionsExact identifier
Phendimetrazine TartratePHENDIMETRAZINE TARTRATEBryant Ranch Prepack1c2370fd-6b40-48dc-a42d-2488041d5b372024-08-08Warnings, Adverse reactionsExact identifier
Phendimetrazine TartratePHENDIMETRAZINE TARTRATEA-S Medication Solutions7adaf128-fef4-4bbf-8b4a-875fe46bf68a2023-07-18Warnings, 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.

DailyMed Product Concepts#

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

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52959-282-07Phendimetrazine Tartrate7 in 1 BOTTLETABLET72
52959-282-14Phendimetrazine Tartrate14 in 1 BOTTLETABLET142
52959-282-21Phendimetrazine Tartrate21 in 1 BOTTLETABLET212
52959-282-28Phendimetrazine Tartrate28 in 1 BOTTLETABLET282
52959-282-30Phendimetrazine Tartrate30 in 1 BOTTLETABLET302
52959-282-35Phendimetrazine Tartrate35 in 1 BOTTLETABLET352
52959-282-42Phendimetrazine Tartrate42 in 1 BOTTLETABLET422
52959-282-60Phendimetrazine Tartrate60 in 1 BOTTLETABLET602
52959-282-90Phendimetrazine Tartrate90 in 1 BOTTLETABLET902

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
52959-282-14EA - Each52959-2824051d3d8-b903-46c7-a67d-1e5f6403f65e12012-07-24
52959-282-21EA - Each52959-282a8a85b55-a4b9-4817-93ec-b923687c479d12012-07-24
52959-282-28EA - Each52959-282c2a0d0a7-9440-4447-9560-bdfc82cbb01812012-07-24
52959-282-30EA - Each52959-282376ada12-78c2-4cff-84bb-b1ed5d3de55912012-07-24
52959-282-35EA - Each52959-28263bd9178-c68e-4391-a3aa-b1cad205629812012-07-24
52959-282-42EA - Each52959-282dd4bafaf-1e84-46ab-8cb1-e9991fc65ef112012-07-24
52959-282-90EA - Each52959-2820a3a742a-ab34-4120-946b-cbb9cf860d2812012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
PHENDIMETRAZINE TARTRATEACTIVE INGREDIENT6985IP0T80PHENDIMETRAZINE TARTRATE TABLET [H.J. HARKINS COMPANY, INC.]1
PHENDIMETRAZINEACTIVE MOIETYAB2794W8KVPHENDIMETRAZINE TARTRATE TABLET [H.J. HARKINS COMPANY, INC.]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UPHENDIMETRAZINE TARTRATE TABLET [H.J. HARKINS COMPANY, INC.]1
FD&C YELLOW NO. 5INACTIVE INGREDIENTI753WB2F1MPHENDIMETRAZINE TARTRATE TABLET [H.J. HARKINS COMPANY, INC.]1
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XPHENDIMETRAZINE TARTRATE TABLET [H.J. HARKINS COMPANY, INC.]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30PHENDIMETRAZINE TARTRATE TABLET [H.J. HARKINS COMPANY, INC.]1
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4PHENDIMETRAZINE TARTRATE TABLET [H.J. HARKINS COMPANY, INC.]1
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2PHENDIMETRAZINE TARTRATE TABLET [H.J. HARKINS COMPANY, INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52959-282PHENDIMETRAZINE TARTRATE ER (PHENDIMETRAZINE TARTRATE) CAPSULE, EXTENDED RELEASE PHENDIMETRAZINE TARTRATE TABLET [H.J. HARKINS COMPANY, INC.]2Legacy NDC, 9 package rows20180922_49b13acc-c7a9-4f7c-bcc2-2c73fcedab52.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
979543phendimetrazine tartrate 105 MG 24HR Extended Release Oral CapsulePSN49b13acc-c7a9-4f7c-bcc2-2c73fcedab522
979549phendimetrazine tartrate 35 MG Oral TabletPSN49b13acc-c7a9-4f7c-bcc2-2c73fcedab522
97954324 HR phendimetrazine tartrate 105 MG Extended Release Oral CapsuleSCD49b13acc-c7a9-4f7c-bcc2-2c73fcedab522
979549phendimetrazine tartrate 35 MG Oral TabletSCD49b13acc-c7a9-4f7c-bcc2-2c73fcedab522
979543phendimetrazine 105 MG 24 HR Extended Release Oral CapsuleSY49b13acc-c7a9-4f7c-bcc2-2c73fcedab522

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
52959-282-07529590282077 in 1 BOTTLEHistorical
52959-282-145295902821414 in 1 BOTTLEHistorical
52959-282-215295902822121 in 1 BOTTLEHistorical
52959-282-285295902822828 in 1 BOTTLEHistorical
52959-282-305295902823030 in 1 BOTTLEHistorical
52959-282-355295902823535 in 1 BOTTLEHistorical
52959-282-425295902824242 in 1 BOTTLEHistorical
52959-282-605295902826060 in 1 BOTTLEHistorical
52959-282-905295902829090 in 1 BOTTLEHistorical