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 ID: 0378-0087_4255111c-66ea-4343-9401-7faffde9132a
• NDC: 0378-0087
• Product Type: Human Prescription Drug
• Proprietary Name: Maprotiline Hydrochloride
• Generic Name: Maprotiline Hydrochloride
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 1988-10-03
• Marketing Category: ANDA / ANDA
• Application Number: ANDA072285
• Labeler Name: Mylan Pharmaceuticals Inc.
• Substance Name: MAPROTILINE HYDROCHLORIDE
• Active Ingredient Strength: 50 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 0378-0087-01

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0087-01)

• Marketing Start Date: 1988-10-03
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0378-0087-01 [00378008701]

Maprotiline Hydrochloride TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA072285
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1988-10-03

Drug Details

Active Ingredients

Ingredient	Strength
MAPROTILINE HYDROCHLORIDE	50 mg/1

OpenFDA Data

• SPL SET ID: c3ca69e6-1ea0-4c2c-abcb-7264b2e79a87
• Manufacturer:
  • Mylan Pharmaceuticals Inc.
• UNII:
  • 7C8J54PVFI
• RxNorm Concept Unique ID - RxCUI:
  • 1298857
  • 1298870
  • 1298861

NDC Crossover Matching brand name "Maprotiline Hydrochloride" or generic name "Maprotiline Hydrochloride"

NDC	Brand Name	Generic Name
0378-0060	Maprotiline Hydrochloride	maprotiline hydrochloride
0378-0087	Maprotiline Hydrochloride	maprotiline hydrochloride
0378-0092	Maprotiline Hydrochloride	maprotiline hydrochloride