NDC 44567-530

Cisplatin

Cisplatin

Cisplatin is a Intravenous Injection, Powder, Lyophilized, For Solution in the Human Prescription Drug category. It is labeled and distributed by Wg Critical Care, Llc. The primary component is Cisplatin.

Product ID44567-530_1dda0f66-289e-4c7b-95f6-9e1a25473a95
NDC44567-530
Product TypeHuman Prescription Drug
Proprietary NameCisplatin
Generic NameCisplatin
Dosage FormInjection, Powder, Lyophilized, For Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2019-04-05
Marketing CategoryNDA / NDA
Application NumberNDA018057
Labeler NameWG Critical Care, LLC
Substance NameCISPLATIN
Active Ingredient Strength1 mg/mL
Pharm ClassesPlatinum-based Drug [EPC],Platinum-containing Compounds [EXT]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 44567-530-01

1 VIAL in 1 CARTON (44567-530-01) > 50 mL in 1 VIAL
Marketing Start Date2019-04-05
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 44567-530-01 [44567053001]

Cisplatin INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Marketing CategoryNDA
Application NumberNDA018057
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-04-05

Drug Details

Active Ingredients

IngredientStrength
CISPLATIN1 mg/mL

OpenFDA Data

SPL SET ID:508496cb-3441-46b3-a4fe-e0d440e6adc6
Manufacturer
UNII

Pharmacological Class

  • Platinum-based Drug [EPC]
  • Platinum-containing Compounds [EXT]

NDC Crossover Matching brand name "Cisplatin" or generic name "Cisplatin"

NDCBrand NameGeneric Name
0143-9504CISplatinCisplatin
0143-9505CISplatinCisplatin
0703-5747CisplatinCisplatin
0703-5748CisplatinCisplatin
16729-288CisplatinCisplatin
44567-509CISplatinCISplatin
44567-510CISplatinCISplatin
44567-511CISplatinCISplatin
44567-530Cisplatincisplatin
47781-609Cisplatincisplatin
47781-610Cisplatincisplatin
63323-103CisplatinCISPLATIN
68001-283CisplatinCisplatin
68083-162CISPLATINCisplatin
68083-163CISPLATINCisplatin
70860-206Cisplatincisplatin
61126-003Platinolcisplatin
61126-004Platinol-AQcisplatin

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