up and up acetaminophen extra strength is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Target Corporation. The primary component is Acetaminophen.
Product ID | 11673-484_5060ccde-cf1e-404c-873f-b71289863eb6 |
NDC | 11673-484 |
Product Type | Human Otc Drug |
Proprietary Name | up and up acetaminophen extra strength |
Generic Name | Acetaminophen |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2009-12-02 |
Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
Application Number | part343 |
Labeler Name | Target Corporation |
Substance Name | ACETAMINOPHEN |
Active Ingredient Strength | 500 mg/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2009-12-02 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC monograph not final |
Application Number | part343 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-12-02 |
Marketing Category | OTC monograph not final |
Application Number | part343 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-03-27 |
Marketing Category | OTC monograph not final |
Application Number | part343 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-12-02 |
Marketing Category | OTC monograph not final |
Application Number | part343 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2014-09-19 |
Marketing Category | OTC monograph not final |
Application Number | part343 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-12-02 |
Marketing End Date | 2013-10-25 |
Marketing Category | OTC monograph not final |
Application Number | part343 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-12-02 |
Marketing Category | OTC monograph not final |
Application Number | part343 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2011-11-17 |
Marketing Category | OTC monograph not final |
Application Number | part343 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-08-26 |
Marketing Category | OTC monograph not final |
Application Number | part343 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-12-02 |
Ingredient | Strength |
---|---|
ACETAMINOPHEN | 500 mg/1 |
SPL SET ID: | dcbf1eaa-f07f-4b46-a6a4-8c5eb5131605 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
11673-484 | up and up acetaminophen extra strength | up and up acetaminophen extra strength |
0121-0657 | Acetaminophen | Acetaminophen |
0113-7000 | Basic Care acetaminophen | Acetaminophen |
0113-7484 | basic care acetaminophen | Acetaminophen |
0113-7544 | Basic Care Acetaminophen | Acetaminophen |
0113-7130 | basic care childrens pain and fever | Acetaminophen |
0113-0020 | good sense childrens pain and fever | Acetaminophen |
0113-0212 | Good Sense Childrens Pain and Fever | Acetaminophen |
0113-0608 | good sense childrens pain and fever | Acetaminophen |
0113-0998 | Good Sense Childrens Pain and Fever | Acetaminophen |
0113-0161 | Good Sense pain and fever | Acetaminophen |
0113-0397 | Good Sense Pain and Fever | acetaminophen |
0113-0590 | Good Sense Pain and Fever | acetaminophen |
0113-0946 | good sense pain and fever | Acetaminophen |
0113-8959 | Good Sense Pain and Fever | Acetaminophen |
0113-0025 | Good Sense Pain Relief | Acetaminophen |
0113-0044 | Good Sense Pain Relief | Acetaminophen |
0113-0187 | good sense pain relief | Acetaminophen |
0113-0217 | good sense pain relief | Acetaminophen |
0113-0227 | Good Sense Pain Relief | Acetaminophen |
0113-0403 | good sense pain relief | Acetaminophen |
0113-0484 | Good Sense Pain Relief | Acetaminophen |
0113-0518 | good sense pain relief | Acetaminophen |
0113-0544 | good sense pain relief | Acetaminophen |
0113-1889 | good sense pain relief | acetaminophen |
0113-1975 | Good Sense Pain Relief | Acetaminophen |
0031-9301 | Robitussin Direct Sore Throat Pain | acetaminophen |