NDC 67046-472

Metoprolol Tartrate

Metoprolol Tartrate

Metoprolol Tartrate is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Contract Pharmacy Services-pa. The primary component is Metoprolol Tartrate.

Product ID67046-472_7df06f6a-96fa-bfe8-e053-2a91aa0ad0e5
NDC67046-472
Product TypeHuman Prescription Drug
Proprietary NameMetoprolol Tartrate
Generic NameMetoprolol Tartrate
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2017-09-20
Marketing CategoryANDA / ANDA
Application NumberANDA076704
Labeler NameContract Pharmacy Services-PA
Substance NameMETOPROLOL TARTRATE
Active Ingredient Strength25 mg/1
Pharm ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 67046-472-07

7 TABLET, FILM COATED in 1 BLISTER PACK (67046-472-07)
Marketing Start Date2017-09-20
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 67046-472-14 [67046047214]

Metoprolol Tartrate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076704
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-20

NDC 67046-472-20 [67046047220]

Metoprolol Tartrate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076704
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-20

NDC 67046-472-07 [67046047207]

Metoprolol Tartrate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076704
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-20

NDC 67046-472-21 [67046047221]

Metoprolol Tartrate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076704
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-20

NDC 67046-472-30 [67046047230]

Metoprolol Tartrate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076704
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-20

NDC 67046-472-15 [67046047215]

Metoprolol Tartrate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076704
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-20

NDC 67046-472-28 [67046047228]

Metoprolol Tartrate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076704
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-20

NDC 67046-472-60 [67046047260]

Metoprolol Tartrate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076704
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-20

Drug Details

Active Ingredients

IngredientStrength
METOPROLOL TARTRATE25 mg/1

OpenFDA Data

SPL SET ID:59a546ed-8476-a54a-e053-2991aa0a3a0d
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 866924
  • UPC Code
  • 0303780018051
  • Pharmacological Class

    • Adrenergic beta-Antagonists [MoA]
    • beta-Adrenergic Blocker [EPC]
    • Adrenergic beta-Antagonists [MoA]
    • beta-Adrenergic Blocker [EPC]

    NDC Crossover Matching brand name "Metoprolol Tartrate" or generic name "Metoprolol Tartrate"

    NDCBrand NameGeneric Name
    0143-9660Metoprolol TartrateMetoroprolol Tartrate
    0143-9873Metoprolol TartrateMetoprolol Tartrate
    0378-0018Metoprolol Tartratemetoprolol tartrate
    0378-0032Metoprolol Tartratemetoprolol tartrate
    0378-0047Metoprolol Tartratemetoprolol tartrate
    0378-4593Metoprolol Tartratemetoprolol tartrate
    0378-4594Metoprolol Tartratemetoprolol tartrate
    0409-1778Metoprolol TartrateMETOPROLOL TARTRATE
    0409-2016Metoprolol TartrateMETOPROLOL TARTRATE
    0409-2285Metoprolol TartrateMETOPROLOL TARTRATE
    0591-0462Metoprolol Tartratemetoprolol tartrate
    0591-0463Metoprolol Tartratemetoprolol tartrate
    67544-911Metoprolol TartrateMetoprolol Tartrate
    68071-1288Metoprolol TartrateMetoprolol Tartrate
    68071-1795Metoprolol TartrateMetoprolol Tartrate
    68071-1950Metoprolol TartrateMetoprolol Tartrate
    68071-1794Metoprolol TartrateMetoprolol Tartrate
    68071-4014Metoprolol TartrateMetoprolol Tartrate
    68071-3263Metoprolol tartrateMetoprolol tartrate
    68071-3337Metoprolol TartrateMetoprolol Tartrate
    68071-4261Metoprolol TartrateMetoprolol Tartrate
    68071-4084Metoprolol TartrateMetoprolol Tartrate
    68071-4307Metoprolol TartrateMetoprolol Tartrate
    68071-4356Metoprolol TartrateMetoprolol Tartrate
    68071-4309Metoprolol TartrateMetoprolol Tartrate
    68071-4571Metoprolol TartrateMetoprolol Tartrate
    68071-4759Metoprolol TartrateMetoprolol Tartrate
    68071-4747Metoprolol TartrateMetoprolol Tartrate
    68071-4269Metoprolol TartrateMetoprolol Tartrate
    68071-4755Metoprolol TartrateMetoprolol Tartrate
    68071-4634Metoprolol TartrateMetoprolol Tartrate
    68083-131Metoprolol TartrateMetoprolol Tartrate
    68071-4769Metoprolol TartrateMetoprolol Tartrate
    68071-4771Metoprolol TartrateMetoprolol Tartrate
    68151-2896Metoprolol TartrateMetoprolol Tartrate
    68151-4645Metoprolol TartrateMetoprolol Tartrate
    68258-6033Metoprolol TartrateMetoprolol Tartrate
    68645-191Metoprolol TartrateMetoprolol Tartrate
    68645-190Metoprolol TartrateMetoprolol Tartrate
    68788-6786Metoprolol TartrateMetoprolol Tartrate
    68788-6847Metoprolol TartrateMetoprolol Tartrate
    68788-7192Metoprolol TartrateMetoprolol Tartrate
    68788-6907Metoprolol TartrateMetoprolol Tartrate
    68788-8932Metoprolol TartrateMetoprolol Tartrate
    68788-6446Metoprolol TartrateMetoprolol Tartrate
    68788-7200Metoprolol TartrateMetoprolol Tartrate
    68788-9286Metoprolol TartrateMetoprolol Tartrate
    68788-7338Metoprolol TartrateMetoprolol Tartrate
    68788-9890Metoprolol TartrateMetoprolol Tartrate
    68788-9889Metoprolol TartrateMetoprolol Tartrate

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