Orange Book product · Generic (ANDA)
METHYLDOPA AND HYDROCHLOROTHIAZIDE
HYDROCHLOROTHIAZIDE; METHYLDOPA
At a glance
Apr 08, 1988
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Apr 08, 1988
38 yr 9 mo ago
Today
Pharmaceutical detail
Active ingredient
HYDROCHLOROTHIAZIDE; METHYLDOPA
Strength
30MG;500MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
ANDA 071821
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of HYDROCHLOROTHIAZIDE; METHYLDOPA
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ANDA 072509 · DAVA PHARMS INC
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ANDA 072510 · DAVA PHARMS INC
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ANDA 070958 · WATSON LABS
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ANDA 070960 · WATSON LABS
- 1989METHYLDOPA AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 070959 · WATSON LABS
- 1989METHYLDOPA AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 071069 · WATSON LABS
- 1988METHYLDOPA AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 071920 · WATSON LABS
- 1988METHYLDOPA AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 071921 · WATSON LABS
- 1988METHYLDOPA AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 071922 · WATSON LABS
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.
