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FDA Drug Approval, A088803, LIDOCAINE HYDROCHLORIDE
FDA Drug Approval, A088803, LIDOCAINE HYDROCHLORIDE
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ANDA: 088803
Company: HIKMA
Drug Name: LIDOCAINE HYDROCHLORIDE
Active Ingredients: LIDOCAINE HYDROCHLORIDE
Strength: 4%
Dosage Form/Route: SOLUTION;TOPICAL
Action Date: 04/03/1985
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AT
Company: HIKMA
Drug Name: LIDOCAINE HYDROCHLORIDE
Active Ingredients: LIDOCAINE HYDROCHLORIDE
Strength: 4%
Dosage Form/Route: SOLUTION;TOPICAL
Action Date: 04/03/1985
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AT
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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