Dr Reddys Company Profile

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DR REDDYS has two hundred and eighty-three approved drugs.

There are twenty-four tentative approvals on DR REDDYS drugs.

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Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	TE	Type	RLD	RS	Patent No.	Patent Expiration	Product	Substance	Delist Req.	Exclusivity Expiration
Dr Reddys Labs Ltd	OLANZAPINE	olanzapine	TABLET;ORAL	076255-003	Apr 23, 2012	AB	RX	No	No		⤷ Try a Trial				⤷ Try a Trial
Dr Reddys Labs Sa	BIORPHEN	phenylephrine hydrochloride	SOLUTION;INTRAVENOUS	212909-001	Oct 21, 2019		RX	Yes	Yes		⤷ Try a Trial				⤷ Try a Trial
Dr Reddys Labs Ltd	CIPROFLOXACIN HYDROCHLORIDE	ciprofloxacin hydrochloride	TABLET;ORAL	075593-001	Jun 9, 2004	AB	RX	No	No		⤷ Try a Trial				⤷ Try a Trial
Dr Reddys	COLESEVELAM HYDROCHLORIDE	colesevelam hydrochloride	TABLET;ORAL	210889-001	Oct 5, 2018	AB	RX	No	No		⤷ Try a Trial				⤷ Try a Trial
Dr Reddys	PROPOFOL	propofol	INJECTABLE;INJECTION	205067-001	Nov 15, 2018	AB	RX	No	No		⤷ Try a Trial				⤷ Try a Trial
Dr Reddys	NEOSTIGMINE METHYLSULFATE	neostigmine methylsulfate	SOLUTION;INTRAVENOUS	209135-001	Jul 10, 2018	AP	RX	No	No		⤷ Try a Trial				⤷ Try a Trial
>Applicant	>Tradename	>Generic Name	>Dosage	>NDA	>Approval Date	>TE	>Type	>RLD	>RS	>Patent No.	>Patent Expiration	>Product	>Substance	>Delist Req.	>Exclusivity Expiration

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Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	Patent No.	Patent Expiration
Dr Reddys Labs Sa	HABITROL	nicotine	FILM, EXTENDED RELEASE;TRANSDERMAL	020076-004	Nov 12, 1999	5,834,011	⤷ Try a Trial
Dr Reddys Labs Sa	HABITROL	nicotine	FILM, EXTENDED RELEASE;TRANSDERMAL	020076-004	Nov 12, 1999	4,597,961	⤷ Try a Trial
Dr Reddys Labs Sa	HABITROL	nicotine	FILM, EXTENDED RELEASE;TRANSDERMAL	020076-005	Nov 12, 1999	5,834,011	⤷ Try a Trial
Dr Reddys Labs Sa	HABITROL	nicotine	FILM, EXTENDED RELEASE;TRANSDERMAL	020076-006	Nov 12, 1999	5,834,011	⤷ Try a Trial
Dr Reddys Labs Sa	HABITROL	nicotine	FILM, EXTENDED RELEASE;TRANSDERMAL	020076-006	Nov 12, 1999	5,016,652	⤷ Try a Trial
Dr Reddys Labs Sa	HABITROL	nicotine	FILM, EXTENDED RELEASE;TRANSDERMAL	020076-006	Nov 12, 1999	4,597,961	⤷ Try a Trial
>Applicant	>Tradename	>Generic Name	>Dosage	>NDA	>Approval Date	>Patent No.	>Patent Expiration

Drugname	Dosage	Strength	Tradename	Submissiondate
➤ Subscribe	for Injection	100 mcg/vial and 500 mcg/vial	➤ Subscribe	2015-04-14
➤ Subscribe	Delayed-release Tablets	20 mg	➤ Subscribe	2015-06-03
➤ Subscribe	for Injection	200 mcg/vial	➤ Subscribe	2015-05-01

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