NDC 0641-6135

Prochlorperazine Edisylate

Prochlorperazine Edisylate

Prochlorperazine Edisylate is a Intramuscular; Intravenous Injection in the Human Prescription Drug category. It is labeled and distributed by Hikma Pharmaceuticals Usa Inc.. The primary component is Prochlorperazine Edisylate.

Product ID0641-6135_0ee79478-7b54-4b31-af4e-f927a996e18c
NDC0641-6135
Product TypeHuman Prescription Drug
Proprietary NameProchlorperazine Edisylate
Generic NameProchlorperazine Edisylate
Dosage FormInjection
Route of AdministrationINTRAMUSCULAR; INTRAVENOUS
Marketing Start Date1989-08-29
Marketing CategoryANDA / ANDA
Application NumberANDA089903
Labeler NameHikma Pharmaceuticals USA Inc.
Substance NamePROCHLORPERAZINE EDISYLATE
Active Ingredient Strength5 mg/mL
Pharm ClassesPhenothiazine [EPC], Phenothiazines [CS]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 0641-6135-25

25 VIAL in 1 CARTON (0641-6135-25) > 2 mL in 1 VIAL (0641-6135-01)
Marketing Start Date1989-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0641-6135-01 [00641613501]

Prochlorperazine Edisylate INJECTION
Marketing CategoryANDA
Application NumberANDA089903
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1989-08-29

NDC 0641-6135-25 [00641613525]

Prochlorperazine Edisylate INJECTION
Marketing CategoryANDA
Application NumberANDA089903
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1989-08-29

Drug Details

Active Ingredients

IngredientStrength
PROCHLORPERAZINE EDISYLATE5 mg/mL

OpenFDA Data

SPL SET ID:baf59816-7577-4652-b065-fb6de9e54569
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 314192
  • Pharmacological Class

    • Phenothiazine [EPC]
    • Phenothiazines [CS]
    • Phenothiazine [EPC]
    • Phenothiazines [CS]

    NDC Crossover Matching brand name "Prochlorperazine Edisylate" or generic name "Prochlorperazine Edisylate"

    NDCBrand NameGeneric Name
    0641-0491Prochlorperazine EdisylateProchlorperazine Edisylate
    0641-6135Prochlorperazine EdisylateProchlorperazine Edisylate
    0713-0351Prochlorperazine EdisylateProchlorperazine Edisylate
    14789-700Prochlorperazine EdisylateProchlorperazine Edisylate
    23155-294Prochlorperazine EdisylateProchlorperazine Edisylate
    23155-497PROCHLORPERAZINE EDISYLATEPROCHLORPERAZINE EDISYLATE
    23155-523Prochlorperazine EdisylateProchlorperazine Edisylate
    25021-790PROCHLORPERAZINE EDISYLATEPROCHLORPERAZINE EDISYLATE
    43066-090PROCHLORPERAZINE EDISYLATEprochlorperazine edisylate
    50090-4548Prochlorperazine EdisylateProchlorperazine Edisylate
    51662-1558PROCHLORPERAZINE EDISYLATEPROCHLORPERAZINE EDISYLATE
    55150-360Prochlorperazine EdisylateProchlorperazine Edisylate
    55154-4183Prochlorperazine EdisylateProchlorperazine Edisylate
    65145-119Prochlorperazine EdisylateProchlorperazine Edisylate
    67457-640prochlorperazine edisylateprochlorperazine edisylate
    68083-435Prochlorperazine EdisylateProchlorperazine Edisylate
    68083-436Prochlorperazine EdisylateProchlorperazine Edisylate
    70121-1580prochlorperazine edisylateprochlorperazine edisylate
    70860-778Prochlorperazine Edisylateprochlorperazine edisylate
    72572-580Prochlorperazine EdisylateProchlorperazine Edisylate

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