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Caffeine
Caffeine - 59779-226-21 - (Caffeine)
Drug Information of Caffeine
| Product NDC: | 59779-226 |
| Proprietary Name: | Caffeine |
| Non Proprietary Name: | Caffeine |
| Active Ingredient(s): | 200 mg/1 & nbsp; Caffeine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Caffeine
| Product NDC: | 59779-226 |
| Labeler Name: | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part340 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19921121 |
Package Information of Caffeine
| Package NDC: | 59779-226-21 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (59779-226-21) > 16 TABLET in 1 BLISTER PACK |
NDC Information of Caffeine
| NDC Code | 59779-226-21 |
| Proprietary Name | Caffeine |
| Package Description | 1 BLISTER PACK in 1 CARTON (59779-226-21) > 16 TABLET in 1 BLISTER PACK |
| Product NDC | 59779-226 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Caffeine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19921121 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
| Substance Name | CAFFEINE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
