| Product NDC: | 62211-023 |
| Proprietary Name: | Children Acetaminophen |
| Non Proprietary Name: | Children Acetaminophen |
| Active Ingredient(s): | 80 mg/1 & nbsp; Children Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 62211-023 |
| Labeler Name: | A&Z Pharmaceutical, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20030310 |
| Package NDC: | 62211-023-99 |
| Package Description: | 37500 TABLET, CHEWABLE in 1 CARTON (62211-023-99) |
| NDC Code | 62211-023-99 |
| Proprietary Name | Children Acetaminophen |
| Package Description | 37500 TABLET, CHEWABLE in 1 CARTON (62211-023-99) |
| Product NDC | 62211-023 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Children Acetaminophen |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20030310 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | A&Z Pharmaceutical, Inc. |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 80 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |