NDC 71369-020

DOPTELET

Avatrombopag Maleate

DOPTELET is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Akarx, Inc.. The primary component is Avatrombopag Maleate.

• Product ID: 71369-020_0391dc0b-343d-4c13-bb0b-170be31c3a0a
• NDC: 71369-020
• Product Type: Human Prescription Drug
• Proprietary Name: DOPTELET
• Generic Name: Avatrombopag Maleate
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2018-05-23
• Marketing Category: NDA / NDA
• Application Number: NDA210238
• Labeler Name: AkaRx, Inc.
• Substance Name: AVATROMBOPAG MALEATE
• Active Ingredient Strength: 20 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 71369-020-10

1 BLISTER PACK in 1 CARTON (71369-020-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK (71369-020-11)

• Marketing Start Date: 2018-05-23
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 71369-020-30 [71369002030]

DOPTELET TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA210238
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2018-05-23

NDC 71369-020-10 [71369002010]

DOPTELET TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA210238
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2018-05-23

NDC 71369-020-16 [71369002016]

DOPTELET TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA210238
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2018-05-23

NDC 71369-020-15 [71369002015]

DOPTELET TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA210238
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2018-05-23

NDC 71369-020-11 [71369002011]

DOPTELET TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA210238
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2018-05-23

Drug Details