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Arthritis Pain Reliever
Arthritis Pain Reliever - 51660-333-01 - (Acetaminophen)
Drug Information of Arthritis Pain Reliever
| Product NDC: | 51660-333 |
| Proprietary Name: | Arthritis Pain Reliever |
| Non Proprietary Name: | Acetaminophen |
| Active Ingredient(s): | 650 mg/1 & nbsp; Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Arthritis Pain Reliever
| Product NDC: | 51660-333 |
| Labeler Name: | Ohm Laboratories Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA076200 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020430 |
Package Information of Arthritis Pain Reliever
| Package NDC: | 51660-333-01 |
| Package Description: | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (51660-333-01) |
NDC Information of Arthritis Pain Reliever
| NDC Code | 51660-333-01 |
| Proprietary Name | Arthritis Pain Reliever |
| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (51660-333-01) |
| Product NDC | 51660-333 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20020430 |
| Marketing Category Name | ANDA |
| Labeler Name | Ohm Laboratories Inc. |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 650 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
