Product Details for ANDA 214322
PREGABALIN (PREGABALIN)
50MG
Marketing Status: Prescription
75MG
Marketing Status: Prescription
100MG
Marketing Status: Prescription
150MG
Marketing Status: Prescription
200MG
Marketing Status: Prescription
225MG
Marketing Status: Prescription
300MG
Marketing Status: Prescription
50MG
Marketing Status: Prescription
Active Ingredient: PREGABALIN
Proprietary Name: PREGABALIN
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A214322
Product Number: 001
Approval Date: Jul 15, 2021
Applicant Holder Full Name: CHANGZHOU PHARMACEUTICAL FACTORY
Marketing Status: Prescription
Patent and Exclusivity Information
PREGABALIN (PREGABALIN)
Proprietary Name: PREGABALIN
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A214322
Product Number: 001
Approval Date: Jul 15, 2021
Applicant Holder Full Name: CHANGZHOU PHARMACEUTICAL FACTORY
Marketing Status: Prescription
Patent and Exclusivity Information
75MG
Marketing Status: Prescription
Active Ingredient: PREGABALIN
Proprietary Name: PREGABALIN
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 75MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A214322
Product Number: 002
Approval Date: Jul 15, 2021
Applicant Holder Full Name: CHANGZHOU PHARMACEUTICAL FACTORY
Marketing Status: Prescription
Patent and Exclusivity Information
PREGABALIN (PREGABALIN)
Proprietary Name: PREGABALIN
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 75MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A214322
Product Number: 002
Approval Date: Jul 15, 2021
Applicant Holder Full Name: CHANGZHOU PHARMACEUTICAL FACTORY
Marketing Status: Prescription
Patent and Exclusivity Information
100MG
Marketing Status: Prescription
Active Ingredient: PREGABALIN
Proprietary Name: PREGABALIN
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A214322
Product Number: 003
Approval Date: Jul 15, 2021
Applicant Holder Full Name: CHANGZHOU PHARMACEUTICAL FACTORY
Marketing Status: Prescription
Patent and Exclusivity Information
PREGABALIN (PREGABALIN)
Proprietary Name: PREGABALIN
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A214322
Product Number: 003
Approval Date: Jul 15, 2021
Applicant Holder Full Name: CHANGZHOU PHARMACEUTICAL FACTORY
Marketing Status: Prescription
Patent and Exclusivity Information
150MG
Marketing Status: Prescription
Active Ingredient: PREGABALIN
Proprietary Name: PREGABALIN
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 150MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A214322
Product Number: 004
Approval Date: Jul 15, 2021
Applicant Holder Full Name: CHANGZHOU PHARMACEUTICAL FACTORY
Marketing Status: Prescription
Patent and Exclusivity Information
PREGABALIN (PREGABALIN)
Proprietary Name: PREGABALIN
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 150MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A214322
Product Number: 004
Approval Date: Jul 15, 2021
Applicant Holder Full Name: CHANGZHOU PHARMACEUTICAL FACTORY
Marketing Status: Prescription
Patent and Exclusivity Information
200MG
Marketing Status: Prescription
Active Ingredient: PREGABALIN
Proprietary Name: PREGABALIN
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A214322
Product Number: 005
Approval Date: Jul 15, 2021
Applicant Holder Full Name: CHANGZHOU PHARMACEUTICAL FACTORY
Marketing Status: Prescription
Patent and Exclusivity Information
PREGABALIN (PREGABALIN)
Proprietary Name: PREGABALIN
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A214322
Product Number: 005
Approval Date: Jul 15, 2021
Applicant Holder Full Name: CHANGZHOU PHARMACEUTICAL FACTORY
Marketing Status: Prescription
Patent and Exclusivity Information
225MG
Marketing Status: Prescription
Active Ingredient: PREGABALIN
Proprietary Name: PREGABALIN
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 225MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A214322
Product Number: 006
Approval Date: Jul 15, 2021
Applicant Holder Full Name: CHANGZHOU PHARMACEUTICAL FACTORY
Marketing Status: Prescription
Patent and Exclusivity Information
PREGABALIN (PREGABALIN)
Proprietary Name: PREGABALIN
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 225MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A214322
Product Number: 006
Approval Date: Jul 15, 2021
Applicant Holder Full Name: CHANGZHOU PHARMACEUTICAL FACTORY
Marketing Status: Prescription
Patent and Exclusivity Information
300MG
Marketing Status: Prescription
Active Ingredient: PREGABALIN
Proprietary Name: PREGABALIN
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 300MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A214322
Product Number: 007
Approval Date: Jul 15, 2021
Applicant Holder Full Name: CHANGZHOU PHARMACEUTICAL FACTORY
Marketing Status: Prescription
Patent and Exclusivity Information
Proprietary Name: PREGABALIN
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 300MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A214322
Product Number: 007
Approval Date: Jul 15, 2021
Applicant Holder Full Name: CHANGZHOU PHARMACEUTICAL FACTORY
Marketing Status: Prescription
Patent and Exclusivity Information