NDC 68788-7448

Desvenlafaxine Succinate

Desvenlafaxine Succinate

Desvenlafaxine Succinate is a Oral Tablet, Film Coated, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is Desvenlafaxine Succinate.

Product ID68788-7448_61856074-f6fb-43e2-82a5-a2bc92f862c4
NDC68788-7448
Product TypeHuman Prescription Drug
Proprietary NameDesvenlafaxine Succinate
Generic NameDesvenlafaxine Succinate
Dosage FormTablet, Film Coated, Extended Release
Route of AdministrationORAL
Marketing Start Date2019-08-20
Marketing CategoryANDA / ANDA
Application NumberANDA204172
Labeler NamePreferred Pharmaceuticals Inc.
Substance NameDESVENLAFAXINE SUCCINATE
Active Ingredient Strength50 mg/1
Pharm ClassesNorepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA],Cytochrome P450 2D6 Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 68788-7448-1

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-7448-1)
Marketing Start Date2019-08-20
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68788-7448-9 [68788744809]

Desvenlafaxine Succinate TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA204172
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-08-20

NDC 68788-7448-1 [68788744801]

Desvenlafaxine Succinate TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA204172
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-08-20

NDC 68788-7448-3 [68788744803]

Desvenlafaxine Succinate TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA204172
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-08-20

NDC 68788-7448-6 [68788744806]

Desvenlafaxine Succinate TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA204172
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-08-20

Drug Details

Active Ingredients

IngredientStrength
DESVENLAFAXINE SUCCINATE50 mg/1

OpenFDA Data

SPL SET ID:a84236bd-4c66-47a7-82bd-83cb857181d3
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1874559
  • Pharmacological Class

    • Norepinephrine Uptake Inhibitors [MoA]
    • Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
    • Serotonin Uptake Inhibitors [MoA]
    • Cytochrome P450 2D6 Inhibitors [MoA]

    NDC Crossover Matching brand name "Desvenlafaxine Succinate" or generic name "Desvenlafaxine Succinate"

    NDCBrand NameGeneric Name
    50090-4069Desvenlafaxine Succinatedesvenlafaxine succinate
    59762-1210Desvenlafaxine Succinatedesvenlafaxine succinate
    68180-592Desvenlafaxine SuccinateDesvenlafaxine Succinate
    68180-593Desvenlafaxine SuccinateDesvenlafaxine Succinate
    59762-1211Desvenlafaxine SuccinateDesvenlafaxine Succinate
    59762-1222Desvenlafaxine SuccinateDesvenlafaxine Succinate
    71335-1150Desvenlafaxine SuccinateDesvenlafaxine Succinate
    68788-7448Desvenlafaxine SuccinateDesvenlafaxine Succinate
    71335-1331Desvenlafaxine SuccinateDesvenlafaxine Succinate
    68788-7488Desvenlafaxine SuccinateDesvenlafaxine Succinate
    46708-540DesvenlafaxineDesvenlafaxine Succinate
    46708-541DesvenlafaxineDesvenlafaxine Succinate
    46708-542DesvenlafaxineDesvenlafaxine Succinate
    50090-5274DesvenlafaxineDesvenlafaxine Succinate
    50090-5293DesvenlafaxineDesvenlafaxine Succinate
    51991-006DesvenlafaxineDesvenlafaxine Succinate
    51991-311DesvenlafaxineDesvenlafaxine Succinate
    51991-312DesvenlafaxineDesvenlafaxine Succinate
    55700-577DesvenlafaxineDesvenlafaxine Succinate
    0008-1210Pristiqdesvenlafaxine succinate
    0008-1211Pristiqdesvenlafaxine succinate
    0008-1222Pristiqdesvenlafaxine succinate
    35356-491Pristiqdesvenlafaxine succinate
    43063-262Pristiqdesvenlafaxine succinate
    55154-4230Pristiqdesvenlafaxine succinate
    55154-4235Pristiqdesvenlafaxine succinate

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