NDC 55289-581

Cimetidine

Cimetidine

Cimetidine is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Pd-rx Pharmaceuticals, Inc.. The primary component is Cimetidine.

Product ID55289-581_7aba96aa-f7a7-1ce3-e053-2a91aa0a6405
NDC55289-581
Product TypeHuman Prescription Drug
Proprietary NameCimetidine
Generic NameCimetidine
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date1994-05-17
Marketing CategoryANDA / ANDA
Application NumberANDA074246
Labeler NamePD-Rx Pharmaceuticals, Inc.
Substance NameCIMETIDINE
Active Ingredient Strength400 mg/1
Pharm ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 55289-581-10

10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-581-10)
Marketing Start Date2015-11-02
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 55289-581-60 [55289058160]

Cimetidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA074246
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-11-02

NDC 55289-581-90 [55289058190]

Cimetidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA074246
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-11-02

NDC 55289-581-20 [55289058120]

Cimetidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA074246
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-11-02

NDC 55289-581-30 [55289058130]

Cimetidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA074246
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-11-02

NDC 55289-581-10 [55289058110]

Cimetidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA074246
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-11-02

Drug Details

Active Ingredients

IngredientStrength
CIMETIDINE400 mg/1

OpenFDA Data

SPL SET ID:28fd7158-a617-436a-8f5c-71ffbaafe527
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197507
  • UPC Code
  • 0355289581109
  • Pharmacological Class

    • Histamine H2 Receptor Antagonists [MoA]
    • Histamine-2 Receptor Antagonist [EPC]

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

    NDCBrand NameGeneric Name
    0093-8192CimetidineCimetidine
    0093-8204CimetidineCimetidine
    0093-8305CimetidineCimetidine
    0121-0649CimetidineCimetidine Hydrochloride
    0121-1298CimetidineCimetidine Hydrochloride
    0363-0022cimetidineCimetidine
    0378-0053Cimetidinecimetidine
    0378-0317Cimetidinecimetidine
    0378-0372Cimetidinecimetidine
    0378-0541Cimetidinecimetidine
    0440-1282CIMETIDINECIMETIDINE
    10544-626CimetidineCimetidine
    10544-627CimetidineCimetidine
    33261-024CimetidineCimetidine
    68151-1742CimetidineCimetidine
    68151-1497CimetidineCimetidine
    68151-2899CimetidineCimetidine
    68788-9064CimetidineCimetidine
    42291-217CimetidineCimetidine
    42291-218CimetidineCimetidine
    50090-0500CimetidineCimetidine
    55289-581CimetidineCimetidine
    63187-333CimetidineCimetidine
    63629-1783CimetidineCimetidine
    63629-1497CimetidineCimetidine
    66267-057CimetidineCimetidine
    66336-945CimetidineCimetidine
    50090-3574CimetidineCimetidine
    50090-0499CimetidineCimetidine
    70518-2809CimetidineCimetidine
    30142-323Acid ReducerCimetidine
    24385-111Good Neighbor Pharmacy Heartburn ReliefCimetidine
    0113-0022Good Sense Heartburn ReliefCimetidine
    36800-022TopCare Heartburn ReliefCimetidine

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