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EXCEDRIN
EXCEDRIN - 0067-8103-92 - (Acetaminophen, Aspirin (NSAID) and Caffeine)
Drug Information of EXCEDRIN
| Product NDC: | 0067-8103 |
| Proprietary Name: | EXCEDRIN |
| Non Proprietary Name: | Acetaminophen, Aspirin (NSAID) and Caffeine |
| Active Ingredient(s): | 250; 250; 65 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Aspirin (NSAID) and Caffeine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of EXCEDRIN
| Product NDC: | 0067-8103 |
| Labeler Name: | Novartis Consumer Health, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075794 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121022 |
Package Information of EXCEDRIN
| Package NDC: | 0067-8103-92 |
| Package Description: | 1 BOTTLE in 1 CARTON (0067-8103-92) > 200 TABLET, FILM COATED in 1 BOTTLE |
NDC Information of EXCEDRIN
| NDC Code | 0067-8103-92 |
| Proprietary Name | EXCEDRIN |
| Package Description | 1 BOTTLE in 1 CARTON (0067-8103-92) > 200 TABLET, FILM COATED in 1 BOTTLE |
| Product NDC | 0067-8103 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Aspirin (NSAID) and Caffeine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20121022 |
| Marketing Category Name | ANDA |
| Labeler Name | Novartis Consumer Health, Inc. |
| Substance Name | ACETAMINOPHEN; ASPIRIN; CAFFEINE |
| Strength Number | 250; 250; 65 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
