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Ringl
Ringl - 49873-082-01 - (acetaminophen)
Drug Information of Ringl
| Product NDC: | 49873-082 |
| Proprietary Name: | Ringl |
| Non Proprietary Name: | acetaminophen |
| Active Ingredient(s): | 325 mg/1 & nbsp; acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ringl
| Product NDC: | 49873-082 |
| Labeler Name: | Sato Pharmaceutical Co., Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19960509 |
Package Information of Ringl
| Package NDC: | 49873-082-01 |
| Package Description: | 1 BOTTLE in 1 CARTON (49873-082-01) > 30 TABLET in 1 BOTTLE |
NDC Information of Ringl
| NDC Code | 49873-082-01 |
| Proprietary Name | Ringl |
| Package Description | 1 BOTTLE in 1 CARTON (49873-082-01) > 30 TABLET in 1 BOTTLE |
| Product NDC | 49873-082 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19960509 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Sato Pharmaceutical Co., Ltd. |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 325 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
