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Clomipramine hydrochloride - Medication Information

Product NDC Code 70771-1014
Drug Name

Clomipramine hydrochloride

Type Generic
Pharm Class Tricyclic Antidepressant [EPC]
Active Ingredients
Clomipramine hydrochloride 75 mg/1
Route ORAL
Dosage Form CAPSULE
RxCUI drug identifier 857297,
857301,
857305
Application Number ANDA208961
Labeler Name Zydus Lifesciences Limited
Packages
Package NDC Code Description
70771-1014-1 100 capsule in 1 bottle (70771-1014-1)
70771-1014-7 30 capsule in 1 bottle (70771-1014-7)
70771-1014-9 90 capsule in 1 bottle (70771-1014-9)
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Spl product data elements

Usually a list of ingredients in a drug product.
Clomipramine Hydrochloride Clomipramine Hydrochloride CLOMIPRAMINE HYDROCHLORIDE CLOMIPRAMINE ALCOHOL AMMONIA BUTYL ALCOHOL CELLULOSE, MICROCRYSTALLINE D&C RED NO. 28 D&C RED NO. 33 D&C YELLOW NO. 10 FD&C BLUE NO. 1 FD&C RED NO. 40 FERROSOFERRIC OXIDE GELATIN ISOPROPYL ALCOHOL MAGNESIUM STEARATE POTASSIUM HYDROXIDE PROPYLENE GLYCOL SHELLAC SILICON DIOXIDE SODIUM LAURYL SULFATE STARCH, CORN TITANIUM DIOXIDE WATER OPAQUE PINK CAP OPAQUE LIGHT PINK BODY CAPSULE 1065 Clomipramine Hydrochloride Clomipramine Hydrochloride CLOMIPRAMINE HYDROCHLORIDE CLOMIPRAMINE ALCOHOL AMMONIA BUTYL ALCOHOL CELLULOSE, MICROCRYSTALLINE D&C RED NO. 33 FD&C RED NO. 40 FERRIC OXIDE YELLOW FERROSOFERRIC OXIDE GELATIN ISOPROPYL ALCOHOL MAGNESIUM STEARATE POTASSIUM HYDROXIDE PROPYLENE GLYCOL SHELLAC SILICON DIOXIDE SODIUM LAURYL SULFATE STARCH, CORN TITANIUM DIOXIDE WATER OPAQUE YELLOW CAP OPAQUE LIGHT PINK BODY CAPSULE 1066 Clomipramine Hydrochloride Clomipramine Hydrochloride CLOMIPRAMINE HYDROCHLORIDE CLOMIPRAMINE ALCOHOL AMMONIA BUTYL ALCOHOL CELLULOSE, MICROCRYSTALLINE D&C RED NO. 28 D&C RED NO. 33 FD&C BLUE NO. 1 FD&C RED NO. 40 FERROSOFERRIC OXIDE GELATIN ISOPROPYL ALCOHOL MAGNESIUM STEARATE POTASSIUM HYDROXIDE PROPYLENE GLYCOL SHELLAC SILICON DIOXIDE SODIUM LAURYL SULFATE STARCH, CORN TITANIUM DIOXIDE WATER OPAQUE DARK PINK CAP OPAQUE LIGHT PINK BODY CAPSULE 1067

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 70771-1012-1 Clomipramine Hydrochloride Capsules USP, 25 mg R x only 100 Capsules NDC 70771-1013-1 Clomipramine Hydrochloride Capsules USP, 50 mg R x only 100 Capsules NDC 70771-1014-1 Clomipramine Hydrochloride Capsules USP, 75 mg R x only 100 Capsules Clomipramine Hydrochloride Capsules, USP Clomipramine Hydrochloride Capsules, USP Clomipramine Hydrochloride Capsules, USP

Spl medguide

Information about the patient medication guide that accompanies the drug product. Certain drugs must be dispensed with an accompanying medication guide. This field may contain information about when to consult the medication guide and the contents of the medication guide.
SPL MEDGUIDE

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API