Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 209452
Company: DR REDDYS
Company: DR REDDYS
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
SAPROPTERIN DIHYDROCHLORIDE | SAPROPTERIN DIHYDROCHLORIDE | 100MG/PACKET | POWDER;ORAL | Prescription | AB | No | No |
Original Approvals or Tentative Approvals
Action Date | Submission | Action Type | Submission Classification | Review Priority; Orphan Status | Letters, Reviews, Labels, Patient Package Insert | Notes | Url |
---|---|---|---|---|---|---|---|
03/30/2021 | ORIG-1 | Approval | STANDARD |
Letter (PDF)
|
Label is not available on this site. |
https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2020/209452Orig1s000TAltr.pdf |
Supplements
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
---|---|---|---|---|---|
03/15/2024 | SUPPL-6 | Labeling-Package Insert, Labeling-Patient Package Insert |
Label is not available on this site. |
||
05/17/2022 | SUPPL-1 | Labeling-Container/Carton Labels, Labeling-Package Insert, Labeling-Proprietary Name Change |
Label is not available on this site. |
SAPROPTERIN DIHYDROCHLORIDE
POWDER;ORAL; 100MG/PACKET
TE Code = AB
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | RLD | TE Code | Application No. | Company |
---|---|---|---|---|---|---|---|---|
KUVAN | SAPROPTERIN DIHYDROCHLORIDE | 100MG/PACKET | POWDER;ORAL | Prescription | Yes | AB | 205065 | BIOMARIN PHARM |
SAPROPTERIN DIHYDROCHLORIDE | SAPROPTERIN DIHYDROCHLORIDE | 100MG/PACKET | POWDER;ORAL | Prescription | No | AB | 215420 | ANNORA PHARMA |
SAPROPTERIN DIHYDROCHLORIDE | SAPROPTERIN DIHYDROCHLORIDE | 100MG/PACKET | POWDER;ORAL | Prescription | No | AB | 209452 | DR REDDYS |
SAPROPTERIN DIHYDROCHLORIDE | SAPROPTERIN DIHYDROCHLORIDE | 100MG/PACKET | POWDER;ORAL | Prescription | No | AB | 207207 | ENDO OPERATIONS |