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ASPIRIN
ASPIRIN - 49483-382-01 - (Aspirin)
Drug Information of ASPIRIN
| Product NDC: | 49483-382 |
| Proprietary Name: | ASPIRIN |
| Non Proprietary Name: | Aspirin |
| Active Ingredient(s): | 500 mg/5001 & nbsp; Aspirin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ASPIRIN
| Product NDC: | 49483-382 |
| Labeler Name: | Time-Cap Labs, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130211 |
Package Information of ASPIRIN
| Package NDC: | 49483-382-01 |
| Package Description: | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (49483-382-01) |
NDC Information of ASPIRIN
| NDC Code | 49483-382-01 |
| Proprietary Name | ASPIRIN |
| Package Description | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (49483-382-01) |
| Product NDC | 49483-382 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aspirin |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130211 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Time-Cap Labs, Inc |
| Substance Name | ASPIRIN |
| Strength Number | 500 |
| Strength Unit | mg/5001 |
| Pharmaceutical Classes |
