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CAFFEINE CITRATE
CAFFEINE CITRATE - 47335-290-44 - (CAFFEINE CITRATE)
Drug Information of CAFFEINE CITRATE
| Product NDC: | 47335-290 |
| Proprietary Name: | CAFFEINE CITRATE |
| Non Proprietary Name: | CAFFEINE CITRATE |
| Active Ingredient(s): | 20 mg/mL & nbsp; CAFFEINE CITRATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CAFFEINE CITRATE
| Product NDC: | 47335-290 |
| Labeler Name: | Sun Pharma Global FZE |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090357 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091001 |
Package Information of CAFFEINE CITRATE
| Package NDC: | 47335-290-44 |
| Package Description: | 10 VIAL, SINGLE-DOSE in 1 CONTAINER (47335-290-44) > 3 mL in 1 VIAL, SINGLE-DOSE (47335-290-40) |
NDC Information of CAFFEINE CITRATE
| NDC Code | 47335-290-44 |
| Proprietary Name | CAFFEINE CITRATE |
| Package Description | 10 VIAL, SINGLE-DOSE in 1 CONTAINER (47335-290-44) > 3 mL in 1 VIAL, SINGLE-DOSE (47335-290-40) |
| Product NDC | 47335-290 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CAFFEINE CITRATE |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20091001 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharma Global FZE |
| Substance Name | CAFFEINE CITRATE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Methylxanthine [EPC],Xanthines [Chemical/Ingredient] |
