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mapap arthritis pain
mapap arthritis pain - 76237-282-30 - (Acetaminophen)
Drug Information of mapap arthritis pain
| Product NDC: | 76237-282 |
| Proprietary Name: | mapap arthritis pain |
| 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 mapap arthritis pain
| Product NDC: | 76237-282 |
| Labeler Name: | McKesson Contract Packaging |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075077 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130409 |
Package Information of mapap arthritis pain
| Package NDC: | 76237-282-30 |
| Package Description: | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-282-30) > 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of mapap arthritis pain
| NDC Code | 76237-282-30 |
| Proprietary Name | mapap arthritis pain |
| Package Description | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-282-30) > 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 76237-282 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20130409 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson Contract Packaging |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 650 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
