NDC 51662-1242

NALOXONE HCI

Naloxone Hci

NALOXONE HCI is a Intramuscular; Intravenous; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Hf Acquisition Co. Llc, Dba Health First. The primary component is Naloxone Hydrochloride.

Product ID51662-1242_80625ecc-d6b5-74fc-e053-2991aa0a4776
NDC51662-1242
Product TypeHuman Prescription Drug
Proprietary NameNALOXONE HCI
Generic NameNaloxone Hci
Dosage FormInjection, Solution
Route of AdministrationINTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Marketing Start Date2018-08-18
Marketing CategoryANDA / ANDA
Application NumberANDA070254
Labeler NameHF Acquisition Co. LLC, DBA Health First
Substance NameNALOXONE HYDROCHLORIDE
Active Ingredient Strength0 mg/mL
Pharm ClassesOpioid Antagonist [EPC],Opioid Antagonists [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 51662-1242-1

1 mL in 1 VIAL (51662-1242-1)
Marketing Start Date2018-08-18
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 51662-1242-1 [51662124201]

NALOXONE HCI INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA070254
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-08-18

Drug Details

Active Ingredients

IngredientStrength
NALOXONE HYDROCHLORIDE.4 mg/mL

OpenFDA Data

SPL SET ID:73c1bad3-6ac3-8682-e053-2a91aa0a176a
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1659929
  • Pharmacological Class

    • Opioid Antagonist [EPC]
    • Opioid Antagonists [MoA]

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