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BUFFERIN
BUFFERIN - 0067-6424-13 - (ASPIRIN)
Drug Information of BUFFERIN
| Product NDC: | 0067-6424 |
| Proprietary Name: | BUFFERIN |
| Non Proprietary Name: | ASPIRIN |
| Active Ingredient(s): | 81 mg/1 & nbsp; ASPIRIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BUFFERIN
| Product NDC: | 0067-6424 |
| Labeler Name: | Novartis Consumer Health, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110311 |
Package Information of BUFFERIN
| Package NDC: | 0067-6424-13 |
| Package Description: | 1 BOTTLE in 1 CARTON (0067-6424-13) > 130 TABLET in 1 BOTTLE |
NDC Information of BUFFERIN
| NDC Code | 0067-6424-13 |
| Proprietary Name | BUFFERIN |
| Package Description | 1 BOTTLE in 1 CARTON (0067-6424-13) > 130 TABLET in 1 BOTTLE |
| Product NDC | 0067-6424 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ASPIRIN |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110311 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Novartis Consumer Health, Inc. |
| Substance Name | ASPIRIN |
| Strength Number | 81 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
