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ASPIRIN
ASPIRIN - 51645-717-08 - (ASPIRIN)
Drug Information of ASPIRIN
| Product NDC: | 51645-717 |
| Proprietary Name: | ASPIRIN |
| Non Proprietary Name: | ASPIRIN |
| Active Ingredient(s): | 81 mg/1 & nbsp; ASPIRIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ASPIRIN
| Product NDC: | 51645-717 |
| Labeler Name: | Gemini Pharmaceuticals, Inc. dba Plus Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130110 |
Package Information of ASPIRIN
| Package NDC: | 51645-717-08 |
| Package Description: | 120 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51645-717-08) |
NDC Information of ASPIRIN
| NDC Code | 51645-717-08 |
| Proprietary Name | ASPIRIN |
| Package Description | 120 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51645-717-08) |
| Product NDC | 51645-717 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ASPIRIN |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20130110 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Gemini Pharmaceuticals, Inc. dba Plus Pharmaceuticals |
| Substance Name | ASPIRIN |
| Strength Number | 81 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
