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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 211063

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CHLORTHALIDONE (CHLORTHALIDONE)
25MG
Marketing Status: Prescription
Active Ingredient: CHLORTHALIDONE
Proprietary Name: CHLORTHALIDONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A211063
Product Number: 001
Approval Date: Feb 26, 2019
Applicant Holder Full Name: CHARTWELL RX SCIENCES LLC
Marketing Status:  Prescription
Patent and Exclusivity Information
CHLORTHALIDONE (CHLORTHALIDONE)
50MG
Marketing Status: Prescription
Active Ingredient: CHLORTHALIDONE
Proprietary Name: CHLORTHALIDONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A211063
Product Number: 002
Approval Date: Feb 26, 2019
Applicant Holder Full Name: CHARTWELL RX SCIENCES LLC
Marketing Status:  Prescription
Patent and Exclusivity Information
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