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Ascriptin
Ascriptin - 0067-0143-85 - (Aspirin)
Drug Information of Ascriptin
| Product NDC: | 0067-0143 |
| Proprietary Name: | Ascriptin |
| Non Proprietary Name: | Aspirin |
| Active Ingredient(s): | 500 mg/1 & nbsp; Aspirin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ascriptin
| Product NDC: | 0067-0143 |
| Labeler Name: | Novartis Consumer Health, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20091231 |
Package Information of Ascriptin
| Package NDC: | 0067-0143-85 |
| Package Description: | 1 BOTTLE in 1 CARTON (0067-0143-85) > 85 TABLET, FILM COATED in 1 BOTTLE |
NDC Information of Ascriptin
| NDC Code | 0067-0143-85 |
| Proprietary Name | Ascriptin |
| Package Description | 1 BOTTLE in 1 CARTON (0067-0143-85) > 85 TABLET, FILM COATED in 1 BOTTLE |
| Product NDC | 0067-0143 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aspirin |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20091231 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Novartis Consumer Health, Inc. |
| Substance Name | ASPIRIN |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
