Home
>
National Drug Code (NDC)
>
TYLENOL EXTRA STRENGTH
TYLENOL EXTRA STRENGTH - 66715-9747-2 - (Acetaminophen)
Drug Information of TYLENOL EXTRA STRENGTH
| Product NDC: | 66715-9747 |
| Proprietary Name: | TYLENOL EXTRA STRENGTH |
| Non Proprietary Name: | Acetaminophen |
| Active Ingredient(s): | 500 mg/1 & nbsp; Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TYLENOL EXTRA STRENGTH
| Product NDC: | 66715-9747 |
| Labeler Name: | Lil' Drug Store Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110809 |
Package Information of TYLENOL EXTRA STRENGTH
| Package NDC: | 66715-9747-2 |
| Package Description: | 2 POUCH in 1 CARTON (66715-9747-2) > 2 TABLET, COATED in 1 POUCH |
NDC Information of TYLENOL EXTRA STRENGTH
| NDC Code | 66715-9747-2 |
| Proprietary Name | TYLENOL EXTRA STRENGTH |
| Package Description | 2 POUCH in 1 CARTON (66715-9747-2) > 2 TABLET, COATED in 1 POUCH |
| Product NDC | 66715-9747 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110809 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Lil' Drug Store Products, Inc. |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
