NDC 70529-049

Corvatrol 0.9%

Sodium Chloride

Corvatrol 0.9% is a Intramuscular; Intravenous; Subcutaneous Injection in the Human Prescription Drug category. It is labeled and distributed by It3 Medical Llc. The primary component is Sodium Chloride.

Product ID70529-049_6a2f25ad-b36d-4a24-af05-d173bb55c2fa
NDC70529-049
Product TypeHuman Prescription Drug
Proprietary NameCorvatrol 0.9%
Generic NameSodium Chloride
Dosage FormInjection
Route of AdministrationINTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Marketing Start Date2017-03-01
Marketing CategoryANDA / ANDA
Application NumberANDA088911
Labeler NameIT3 Medical LLC
Substance NameSODIUM CHLORIDE
Active Ingredient Strength9 mg/mL
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 70529-049-01

1 VIAL, MULTI-DOSE in 1 PACKAGE (70529-049-01) > 30 mL in 1 VIAL, MULTI-DOSE
Marketing Start Date2017-03-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70529-049-30 [70529004930]

Corvatrol 0.9% INJECTION
Marketing CategoryANDA
Application NumberANDA088911
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-03-01

NDC 70529-049-35 [70529004935]

Corvatrol 0.9% INJECTION
Marketing CategoryANDA
Application NumberANDA088911
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-03-01

NDC 70529-049-25 [70529004925]

Corvatrol 0.9% INJECTION
Marketing CategoryANDA
Application NumberANDA088911
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-03-01

NDC 70529-049-40 [70529004940]

Corvatrol 0.9% INJECTION
Marketing CategoryANDA
Application NumberANDA088911
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-03-01

NDC 70529-049-01 [70529004901]

Corvatrol 0.9% INJECTION
Marketing CategoryANDA
Application NumberANDA088911
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-03-01

NDC 70529-049-20 [70529004920]

Corvatrol 0.9% INJECTION
Marketing CategoryANDA
Application NumberANDA088911
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-03-01

NDC 70529-049-45 [70529004945]

Corvatrol 0.9% INJECTION
Marketing CategoryANDA
Application NumberANDA088911
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-03-01

NDC 70529-049-15 [70529004915]

Corvatrol 0.9% INJECTION
Marketing CategoryANDA
Application NumberANDA088911
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-03-01

Drug Details

Active Ingredients

IngredientStrength
SODIUM CHLORIDE9 mg/mL

OpenFDA Data

SPL SET ID:b344c76d-5ba1-4e1e-9560-deda154e43fe
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 313002

    • NDC Crossover Matching brand name "Corvatrol 0.9%" or generic name "Sodium Chloride"

    NDCBrand NameGeneric Name
    70529-049Corvatrol 0.9%Corvatrol 0.9%
    0220-0432Aqua marinaSODIUM CHLORIDE
    0220-3582Natrum muriaticumSODIUM CHLORIDE
    0220-3583Natrum muriaticumSODIUM CHLORIDE
    0220-3586Natrum muriaticumSODIUM CHLORIDE
    0220-3587Natrum muriaticumSODIUM CHLORIDE
    0220-3590Natrum muriaticumSODIUM CHLORIDE
    0220-3593Natrum muriaticumSODIUM CHLORIDE
    0220-3595Natrum muriaticumSODIUM CHLORIDE
    0220-3596Natrum muriaticumSODIUM CHLORIDE
    0220-3597Natrum muriaticumSODIUM CHLORIDE
    0220-3598Natrum muriaticumSODIUM CHLORIDE
    0220-3599Natrum muriaticumSODIUM CHLORIDE
    0220-3600Natrum muriaticumSODIUM CHLORIDE
    0220-3601Natrum muriaticumSODIUM CHLORIDE
    0019-1188SODIUM CHLORIDEsodium chloride
    0264-1800Sodium ChlorideSodium Chloride
    0264-2201Sodium ChlorideSodium Chloride
    0264-5802Sodium ChlorideSODIUM CHLORIDE
    0264-5804Sodium ChlorideSODIUM CHLORIDE
    0264-7800Sodium ChlorideSodium Chloride
    0264-7802Sodium ChlorideSODIUM CHLORIDE
    0264-7805Sodium ChlorideSodium Chloride
    0264-7806Sodium ChlorideSodium Chloride
    0264-9375Sodium ChlorideSodium Chloride
    0264-9999Sodium ChlorideSodium Chloride
    0338-0043Sodium ChlorideSodium Chloride
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