NDC properties for "Excedrin PM Triple Action Caplets and Excedrin Extra Strength Pain Reliever Kit" (RxCUI 2047428)
About this data
The tables show NDC propoerties for Excedrin PM Triple Action Caplets and Excedrin Extra Strength Pain Reliever Kit with the RxCUI 2047428
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product
Details for Excedrin PM Triple Action Caplets and Excedrin Extra Strength Pain Reliever Kit (RxCUI 2047428)
| RxCUI | 2047428 |
|---|---|
| SPL_SET_ID | 444fa225-c204-45d1-b3b3-aa5650ee5d07 |
| Prescribable Synonym | Excedrin PM Triple Action Caplets and Excedrin Extra Strength Pain Reliever Kit |
| RXNAV_STR | Excedrin PM Triple Action Caplets and Excedrin Extra Strength Pain Reliever Kit |
| RxNorm Name | {100 (acetaminophen 250 MG / aspirin 250 MG / caffeine 65 MG Oral Tablet [Excedrin]) / 24 (acetaminophen 250 MG / aspirin 250 MG / diphenhydramine citrate 38 MG Oral Tablet [Excedrin PM Triple Action]) } Pack [Excedrin PM Triple Action Caplets and Excedrin Extra Strength Pain Reliever] |
| RxNorm Synonym | Excedrin PM Triple Action Caplets and Excedrin Extra Strength Pain Reliever Kit |
| Tallman Synonym | {100 (acetaminophen 250 MG / aspirin 250 MG / caffeine 65 MG Oral Tablet [Excedrin]) / 24 (acetaminophen 250 MG / aspirin 250 MG / diphenhydrAMINE citrate 38 MG Oral Tablet [Excedrin PM Triple Action]) } Pack [Excedrin PM Triple Action Caplets and Excedrin Extra Strength Pain Reliever] |
| Related queries | Interactions (for RxCUI 2047428) |
NDC Properties
NDC Item 00067814801
| NDC 9 | 0067-8148 |
|---|---|
| NDC 10 | 0067-8148-01 |
| NDC Item | 00067814801 |
| Packaging | 1 KIT in 1 PACKAGE, COMBINATION (0067-8148-01) * 1 BOTTLE in 1 CARTON (0067-2056-24) / 24 TABLET, COATED in 1 BOTTLE * 1 BOTTLE in 1 CARTON (0067-2000-91) / 100 TABLET, FILM COATED in 1 BOTTLE |
| FDA SPL set id | 776069 |
| Labeler | Haleon US Holdings LLC |
| Label type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Marketing effective time low | 2018-05-01 |
| Marketing status | ACTIVE |
| OTC_MONOGRAPH_DRUG | M013 |
| Related queries | Properties for NDC 9 0067-8148 |