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FDA Approval Activities for this Drug
Sustiva (Efavirenz) Tablets & Capsules, 600 mg and 50, 100 & 200 mg respectively, Bristol-Myers Squibb NDA 20-972/S-18 & 21-360/S-3 6/10/03 7/8/03 7/8/03
Sustiva (Efavirenz) Tablets & Capsules, 600 mg and 50, 100 & 200 mg respectively, Bristol-Myers Squibb NDA 20-972/S-19 & 21-360/S-4 6/10/03 7/8/03 7/8/03
Sustiva (Efavirenz) Tablets & Capsules, 300 & 600 mg and 50, 100 & 200 mg respectively, Bristol-Myers Squibb NDA 20-972/S-17 & 21-360/S-1 9/20/02 9/27/02
Sustiva (Efavirenz) Tablets, 300 & 600 mg, Bristol-Myers Squibb Pharma Company NDA 21-360 2/1/02 2/27/02 2/4/02 5/15/02
Sustiva (efavirenz) Capsules, 50, 100 & 200 mg, Bristol-Myers Squibb Company NDA 20-972/S-016 1/29/03 2/12/03 2/13/03
Sustiva (efavirenz) Capsules, 50, 100 & 200 mg, DuPont Company NDA 20-972/S13 10/16/01 04/25/03
Sustiva (efavirenz), Bristol-Myers Squibb Company NDA 20-972/S-007 3/1/02 3/5/02
Sustiva (efavirenz), 50mg, 100mg, 200mg capsules (Group Leader Memo)
(Divison Director Memo) DuPont Company NDA 20-972 9/17/98 9/24/98 9/17/98 12/10
Sustiva (efavirenz), 50 mg, 100 mg, and 200 mg capsules DuPont Company NDA 20-972/SE7-001 2/9/00 2/14/00
Sustiva Indication:For the treatment of HIV-1 infection Sustiva (Efavirenz) Capsules & Tablets, Bristol-Myers Squibb SUSTIVA (efavirenz) Capsules, Bristol-Myers Squibb, Efficacy Supplement with Clinical Data to Support
SUSTIVA (efavirenz) Tablets, Bristol-Myers Squibb, Efficacy Supplement with Clinical Data to Support | Sustiva (efavirenz) tablets, GlaxoSmithKline, Labeling Revision |
Sustiva (efavirenz) capsules, GlaxoSmithKline, Labeling Revision | SUSTIVA (efavirenz) Capsules, Bristol-Myers Squibb, Labeling Revision | SUSTIVA (efavirenz) Tablets, Bristol-Myers Squibb, Labeling Revision
For the most up-to-date approval information, please locate this API using the drug index.
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