NDC 0378-0087

Maprotiline Hydrochloride

Maprotiline Hydrochloride

Maprotiline Hydrochloride is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Mylan Pharmaceuticals Inc.. The primary component is Maprotiline Hydrochloride.

Product ID0378-0087_4255111c-66ea-4343-9401-7faffde9132a
NDC0378-0087
Product TypeHuman Prescription Drug
Proprietary NameMaprotiline Hydrochloride
Generic NameMaprotiline Hydrochloride
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date1988-10-03
Marketing CategoryANDA / ANDA
Application NumberANDA072285
Labeler NameMylan Pharmaceuticals Inc.
Substance NameMAPROTILINE HYDROCHLORIDE
Active Ingredient Strength50 mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0378-0087-01

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0087-01)
Marketing Start Date1988-10-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0378-0087-01 [00378008701]

Maprotiline Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA072285
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1988-10-03

Drug Details

Active Ingredients

IngredientStrength
MAPROTILINE HYDROCHLORIDE50 mg/1

OpenFDA Data

SPL SET ID:c3ca69e6-1ea0-4c2c-abcb-7264b2e79a87
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1298857
  • 1298870
  • 1298861
  • NDC Crossover Matching brand name "Maprotiline Hydrochloride" or generic name "Maprotiline Hydrochloride"

    NDCBrand NameGeneric Name
    0378-0060Maprotiline Hydrochloridemaprotiline hydrochloride
    0378-0087Maprotiline Hydrochloridemaprotiline hydrochloride
    0378-0092Maprotiline Hydrochloridemaprotiline hydrochloride

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