NDC 43538-173

Clindacin ETZ

Clindamycin Phosphate

Clindacin ETZ is a Kit in the Human Prescription Drug category. It is labeled and distributed by Medimetriks Pharmaceuticals, Inc.. The primary component is .

Product ID43538-173_fd6c8795-7331-42d6-8a8b-95f9e964b9ee
NDC43538-173
Product TypeHuman Prescription Drug
Proprietary NameClindacin ETZ
Generic NameClindamycin Phosphate
Dosage FormKit
Marketing Start Date2013-06-15
Marketing CategoryANDA / ANDA
Application NumberANDA065049
Labeler NameMedimetriks Pharmaceuticals, Inc.
Active Ingredient Strength0
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 43538-173-60

1 KIT in 1 CARTON (43538-173-60) * 473 mL in 1 BOTTLE * 60 SWAB in 1 CARTON
Marketing Start Date2013-06-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 43538-173-60 [43538017360]

Clindacin ETZ KIT
Marketing CategoryANDA
Application NumberANDA065049
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2013-06-15

Drug Details

OpenFDA Data

SPL SET ID:89fed26e-1cad-4c0b-8695-d6f3562ba8d5
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 797274
  • 1091339
  • Medicade Reported Pricing

    43538017360 CLINDACIN ETZ KIT

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Clindacin ETZ" or generic name "Clindamycin Phosphate"

    NDCBrand NameGeneric Name
    43538-172Clindacin ETZClindacin ETZ
    43538-173Clindacin ETZClindacin ETZ
    0009-0302Cleocin Phosphateclindamycin phosphate
    0009-0602Cleocin Phosphateclindamycin phosphate
    0009-0728Cleocin Phosphateclindamycin phosphate
    0009-0775Cleocin Phosphateclindamycin phosphate
    0009-0870Cleocin Phosphateclindamycin phosphate

    Trademark Results [Clindacin ETZ]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    CLINDACIN ETZ
    CLINDACIN ETZ
    85538104 4419247 Live/Registered
    Medimetriks Pharmaceuticals, Inc.
    2012-02-09

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.