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ConRx Alert
ConRx Alert - 68737-229-13 - (Caffeine)
Drug Information of ConRx Alert
| Product NDC: | 68737-229 |
| Proprietary Name: | ConRx Alert |
| 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 ConRx Alert
| Product NDC: | 68737-229 |
| Labeler Name: | Eagle Distributors,Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part340 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130215 |
Package Information of ConRx Alert
| Package NDC: | 68737-229-13 |
| Package Description: | 50 POUCH in 1 BOX (68737-229-13) > 2 TABLET in 1 POUCH |
NDC Information of ConRx Alert
| NDC Code | 68737-229-13 |
| Proprietary Name | ConRx Alert |
| Package Description | 50 POUCH in 1 BOX (68737-229-13) > 2 TABLET in 1 POUCH |
| Product NDC | 68737-229 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Caffeine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130215 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Eagle Distributors,Inc. |
| Substance Name | CAFFEINE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
