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ACETAMINOPHEN
ACETAMINOPHEN - 51645-601-10 - (ACETAMINOPHEN)
Drug Information of ACETAMINOPHEN
| Product NDC: | 51645-601 |
| Proprietary Name: | ACETAMINOPHEN |
| Non Proprietary Name: | ACETAMINOPHEN |
| Active Ingredient(s): | 500 mg/1 & nbsp; ACETAMINOPHEN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ACETAMINOPHEN
| Product NDC: | 51645-601 |
| Labeler Name: | Gemini Pharmaceuticals, Inc. dba ONDRA Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120330 |
Package Information of ACETAMINOPHEN
| Package NDC: | 51645-601-10 |
| Package Description: | 1000 TABLET in 1 BOTTLE, PLASTIC (51645-601-10) |
NDC Information of ACETAMINOPHEN
| NDC Code | 51645-601-10 |
| Proprietary Name | ACETAMINOPHEN |
| Package Description | 1000 TABLET in 1 BOTTLE, PLASTIC (51645-601-10) |
| Product NDC | 51645-601 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ACETAMINOPHEN |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120330 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Gemini Pharmaceuticals, Inc. dba ONDRA Pharmaceuticals |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
