NDC 68151-0079

Ticlopidine Hydrochloride

Ticlopidine Hydrochloride

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

• Product ID: 68151-0079_c01a9760-cfb9-4d0d-9cf6-12d9deff463f
• NDC: 68151-0079
• 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: 1999-09-07
• Marketing Category: ANDA / ANDA
• Application Number: ANDA075149
• Labeler Name: Carilion Materials Management
• 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 SPL Data Element Entries

NDC 68151-0079-0 [68151007900]

Ticlopidine Hydrochloride TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA075149
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1999-09-07
• Marketing End Date: 2016-07-01
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
TICLOPIDINE HYDROCHLORIDE	250 mg/1

OpenFDA Data

• SPL SET ID: 77d619f8-05a3-408a-a6f8-1511694b6a24
• Manufacturer:
  • Carilion Materials Management
• UNII:
  • A1L4914FMF
• RxNorm Concept Unique ID - RxCUI:
  • 313406

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