NDC 51662-1471

PROPOFOL

Propofol

PROPOFOL is a Intravenous Injection, Emulsion in the Human Prescription Drug category. It is labeled and distributed by Hf Acquisition Co Llc, Dba Healthfirst. The primary component is Propofol.

Product ID51662-1471_99c8438a-2b3d-796e-e053-2a95a90a0200
NDC51662-1471
Product TypeHuman Prescription Drug
Proprietary NamePROPOFOL
Generic NamePropofol
Dosage FormInjection, Emulsion
Route of AdministrationINTRAVENOUS
Marketing Start Date2019-12-15
Marketing CategoryANDA / ANDA
Application NumberANDA077908
Labeler NameHF Acquisition Co LLC, DBA HealthFirst
Substance NamePROPOFOL
Active Ingredient Strength10 mg/mL
Pharm ClassesGeneral Anesthesia [PE],General Anesthetic [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 51662-1471-1

50 mL in 1 VIAL (51662-1471-1)
Marketing Start Date2019-12-15
NDC Exclude FlagN
Sample Package?N

Drug Details

Active Ingredients

IngredientStrength
PROPOFOL10 mg/mL

Pharmacological Class

  • General Anesthesia [PE]
  • General Anesthetic [EPC]

NDC Crossover Matching brand name "PROPOFOL" or generic name "Propofol"

NDCBrand NameGeneric Name
63323-269DiprivanPROPOFOL
65219-800DiprivanPROPOFOL
0409-4699PROPOFOLPROPOFOL
0591-2136PropofolPropofol
25021-608propofolpropofol
51662-1293PROPOFOLPROPOFOL
52584-054PropofolPropofol
52584-699PropofolPropofol
50090-4569PropofolPropofol
51662-1470PROPOFOLPROPOFOL
51662-1471PROPOFOLPROPOFOL

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