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Acetaminophen Extended Release
Acetaminophen Extended Release - 0615-7590-39 - (Acetaminophen)
Drug Information of Acetaminophen Extended Release
| Product NDC: | 0615-7590 |
| Proprietary Name: | Acetaminophen Extended Release |
| Non Proprietary Name: | Acetaminophen |
| Active Ingredient(s): | 650 mg/1 & nbsp; Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Acetaminophen Extended Release
| Product NDC: | 0615-7590 |
| Labeler Name: | NCS HealthCare of KY, Inc dba Vangard Labs |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075077 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20000225 |
Package Information of Acetaminophen Extended Release
| Package NDC: | 0615-7590-39 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (0615-7590-39) |
NDC Information of Acetaminophen Extended Release
| NDC Code | 0615-7590-39 |
| Proprietary Name | Acetaminophen Extended Release |
| Package Description | 30 TABLET in 1 BLISTER PACK (0615-7590-39) |
| Product NDC | 0615-7590 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20000225 |
| Marketing Category Name | ANDA |
| Labeler Name | NCS HealthCare of KY, Inc dba Vangard Labs |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 650 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
