NDC 0185-0115

Ticlopidine Hydrochloride

Ticlopidine Hydrochloride

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

• Product ID: 0185-0115_69bb6c03-a786-4ced-9d02-ee541657f376
• NDC: 0185-0115
• Product Type: Human Prescription Drug
• Proprietary Name: Ticlopidine Hydrochloride
• Generic Name: Ticlopidine Hydrochloride
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 1999-08-20
• Marketing Category: ANDA / ANDA
• Application Number: ANDA075326
• Labeler Name: Eon Labs, Inc.
• Substance Name: TICLOPIDINE HYDROCHLORIDE
• Active Ingredient Strength: 250 mg/1
• Pharm Classes: Decreased Platelet Aggregation [PE],Platelet Aggregation Inhibitor [EPC]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 0185-0115-60

60 TABLET, FILM COATED in 1 BOTTLE (0185-0115-60)

• Marketing Start Date: 1999-08-20
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0185-0115-30 [00185011530]

Ticlopidine Hydrochloride TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA075326
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1999-08-20
• Marketing End Date: 2015-12-31

NDC 0185-0115-60 [00185011560]

Ticlopidine Hydrochloride TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA075326
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1999-08-20
• Marketing End Date: 2015-12-31

NDC 0185-0115-05 [00185011505]

Ticlopidine Hydrochloride TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA075326
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1999-08-20
• Marketing End Date: 2015-12-31

Drug Details

Active Ingredients

Ingredient	Strength
TICLOPIDINE HYDROCHLORIDE	250 mg/1

OpenFDA Data

• SPL SET ID: 0f96e04b-436f-477f-98b3-8668c7ee84ee
• Manufacturer:
  • Eon Labs, Inc.
• UNII:
  • A1L4914FMF
• RxNorm Concept Unique ID - RxCUI:
  • 313406
• UPC Code:
  • 0301850115303

Pharmacological Class

• Decreased Platelet Aggregation [PE]
• Platelet Aggregation Inhibitor [EPC]

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

NDC	Brand Name	Generic Name
0185-0115	Ticlopidine Hydrochloride	Ticlopidine Hydrochloride
57664-327	Ticlopidine Hydrochloride	Ticlopidine Hydrochloride
68151-0079	Ticlopidine Hydrochloride	Ticlopidine Hydrochloride