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Halfprin
Halfprin - 55505-136-01 - (Asprin)
Drug Information of Halfprin
| Product NDC: | 55505-136 |
| Proprietary Name: | Halfprin |
| Non Proprietary Name: | Asprin |
| Active Ingredient(s): | 162 mg/1621 & nbsp; Asprin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Halfprin
| Product NDC: | 55505-136 |
| Labeler Name: | Kramer Laboratories |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20101202 |
Package Information of Halfprin
| Package NDC: | 55505-136-01 |
| Package Description: | 1 TABLET, COATED in 1 POUCH (55505-136-01) |
NDC Information of Halfprin
| NDC Code | 55505-136-01 |
| Proprietary Name | Halfprin |
| Package Description | 1 TABLET, COATED in 1 POUCH (55505-136-01) |
| Product NDC | 55505-136 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Asprin |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20101202 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Kramer Laboratories |
| Substance Name | ASPIRIN |
| Strength Number | 162 |
| Strength Unit | mg/1621 |
| Pharmaceutical Classes |
