Details for New Drug Application (NDA): 090357
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NDA 090357 describes CAFFEINE CITRATE, which is a drug marketed by Am Regent, Eugia Pharma, Exela Pharma Science, Fresenius Kabi Usa, Micro Labs, Sagent Pharms, Sun Pharm, and Exela Pharma, and is included in thirteen NDAs. It is available from seven suppliers. Additional details are available on the CAFFEINE CITRATE profile page.
The generic ingredient in CAFFEINE CITRATE is caffeine citrate. There are eleven drug master file entries for this compound. Eight suppliers are listed for this compound. Additional details are available on the caffeine citrate profile page.
The generic ingredient in CAFFEINE CITRATE is caffeine citrate. There are eleven drug master file entries for this compound. Eight suppliers are listed for this compound. Additional details are available on the caffeine citrate profile page.
Summary for 090357
| Tradename: | CAFFEINE CITRATE |
| Applicant: | Sun Pharm |
| Ingredient: | caffeine citrate |
| Patents: | 0 |
Pharmacology for NDA: 090357
| Physiological Effect | Central Nervous System Stimulation |
Medical Subject Heading (MeSH) Categories for 090357
Suppliers and Packaging for NDA: 090357
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| CAFFEINE CITRATE | caffeine citrate | SOLUTION;ORAL | 090357 | ANDA | Sun Pharmaceutical Industries, Inc. | 47335-290 | 47335-290-44 | 10 VIAL, SINGLE-DOSE in 1 CONTAINER (47335-290-44) / 3 mL in 1 VIAL, SINGLE-DOSE (47335-290-40) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;ORAL | Strength | EQ 30MG BASE/3ML (EQ 10MG BASE/ML) | ||||
| Approval Date: | Sep 30, 2009 | TE: | AA | RLD: | No | ||||
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