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Anacin
Anacin - 63736-211-75 - (Aspirin and Caffeine)
Drug Information of Anacin
| Product NDC: | 63736-211 |
| Proprietary Name: | Anacin |
| Non Proprietary Name: | Aspirin and Caffeine |
| Active Ingredient(s): | 500; 32 mg/1; mg/1 & nbsp; Aspirin and Caffeine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Anacin
| Product NDC: | 63736-211 |
| Labeler Name: | Insight Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090707 |
Package Information of Anacin
| Package NDC: | 63736-211-75 |
| Package Description: | 1 BOTTLE in 1 BOX (63736-211-75) > 75 TABLET, COATED in 1 BOTTLE |
NDC Information of Anacin
| NDC Code | 63736-211-75 |
| Proprietary Name | Anacin |
| Package Description | 1 BOTTLE in 1 BOX (63736-211-75) > 75 TABLET, COATED in 1 BOTTLE |
| Product NDC | 63736-211 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aspirin and Caffeine |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20090707 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Insight Pharmaceuticals |
| Substance Name | ASPIRIN; CAFFEINE |
| Strength Number | 500; 32 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
