Alembic Pharmaceuticals (Alembic) announced that it has received Final Approval from the US Food & Drug Administration (USFDA) for its Abbreviated New Drug Application (ANDA) for Diltiazem ...

Alembic Pharmaceuticals said that it has received final approval from the US Food & Drug Administration (USFDA) for its abbreviated new drug application (ANDA) for Diltiazem Hydrochloride ...

The approval by the US Food & Drug Administration (USFDA) for the abbreviated new drug application (ANDA) for Diltiazem Hydrochloride Extended-Release Capsules of strengths 120 mg, 180 mg, 240 mg, 300 ...

The approval by the US Food & Drug Administration (USFDA) for the abbreviated new drug application (ANDA) for Diltiazem Hydrochloride Extended-Release Capsules of strengths 120 mg, 180 mg, 240 mg, 300 ...

for its generic Diltiazem Hydrochloride extended-release capsules. These capsules are intended to treat hypertension and come in strengths of 120 mg, 180 mg, 240 mg, 300 mg, and 360 mg. The approval ...

for its Abbreviated New Drug Application (ANDA) for Diltiazem Hydrochloride Extended-Release Capsules USP, 120 mg, 180 mg, 240 mg, 300 mg, and 360 mg. According to company’s statement ...

Alembic Pharmaceuticals receives USFDA approval for its generic Diltiazem Hydrochloride extended-release capsules, indicated for hypertension treatment. The approval covers various strengths of the ...

The US Gov­ern­ment Ac­count­abil­i­ty Of­fice pub­lished a new re­port de­tail­ing con­cerns with the staffing of the FDA’s drug in­spec­tion pro­gram, and the fact that the … ...

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These alterations make it harder for people to stop using substances even when they want to, which can lead to drug addiction. It is possible to overcome drug addiction, but it takes commitment and ...

The US health regulator granted final approval for Alembic Pharma's Abbreviated New Drug Application (ANDA) for Ivabradine tablets in 5 mg and 7.5 mg doses. The approved ANDA is a therapeutic ...