27 Dec, 11:59 - Indian

SENSEX 78808.25 (0.43)

Nifty 50 23857.5 (0.45)

Nifty Bank 51402.3984375 (0.45)

Nifty IT 43598.6484375 (-0.15)

Nifty Midcap 100 57049.94921875 (-0.13)

Nifty Next 50 68945.203125 (-0.32)

Nifty Pharma 22933.19921875 (0.97)

Nifty Smallcap 100 18751.25 (0.12)

27 Dec, 11:59 - Global

NIKKEI 225 40280.94 (1.80)

HANG SENG 20088.23 (-0.05)

S&P 6091 (-0.27)


Hot Pursuit News

You are Here : Home > News > Hot Pursuit News >

(21 Sep 2024, 14:05)

Aarti Drugs’ Maharashtra facility gets 7 observations from USFDA

Aarti Drugs announced that the United States Food and Drug Administration (USFDA) conducted an inspection at its active pharmaceutical ingredient (API) manufacturing facility located in MIDC, Tarapur, Maharashtra.


The API inspection was conducted from 12 September to 20 September 2024. At the conclusion of the inspection, the USFDA issued a Form FDA 483, which included seven inspectional observations. Notably, none of the observations were related to data integrity.

The company stated that it will work closely with USFDA to resolve all points raised during the inspection.

Aarti Drugs is primarily involved in manufacturing and marketing of Active Pharmaceutical Ingredients (API), Pharma Intermediates and Specialty Chemicals.

The company’s consolidated net profit declined 30.5% to Rs 33.24 crore on 16% slide in net sales to Rs 555.34 crore in Q1 FY25 over Q1 FY24.

The scrip advanced 1.16% to ends at Rs 524.80 on Friday, 20 September 2024.

More News
More Company News View Company Information