ADVIL PM is a Oral Capsule, Liquid Filled in the Human Otc Drug category. It is labeled and distributed by Pfizer Consumer Healthcare. The primary component is Diphenhydramine Hydrochloride; Ibuprofen.
| Product ID | 0573-0167_61822ea5-d629-442f-bedb-b77115a427d4 |
| NDC | 0573-0167 |
| Product Type | Human Otc Drug |
| Proprietary Name | ADVIL PM |
| Generic Name | Diphenhydramine Hcl, Ibuprofen |
| Dosage Form | Capsule, Liquid Filled |
| Route of Administration | ORAL |
| Marketing Start Date | 2005-12-20 |
| Marketing Category | NDA / NDA |
| Application Number | NDA021393 |
| Labeler Name | Pfizer Consumer Healthcare |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN |
| Active Ingredient Strength | 25 mg/1; mg/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2005-12-20 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA021393 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2005-12-20 |
| Marketing End Date | 2017-12-07 |
| Marketing Category | NDA |
| Application Number | NDA021393 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2005-12-20 |
| Marketing Category | NDA |
| Application Number | NDA021393 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2005-12-20 |
| Marketing End Date | 2017-12-07 |
| Marketing Category | NDA |
| Application Number | NDA021393 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2005-12-20 |
| Marketing End Date | 2017-12-07 |
| Marketing Category | NDA |
| Application Number | NDA021393 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2005-12-20 |
| Marketing Category | NDA |
| Application Number | NDA021393 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2005-12-20 |
| Marketing End Date | 2017-12-07 |
| Marketing Category | NDA |
| Application Number | NDA021393 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2005-12-20 |
| Marketing Category | NDA |
| Application Number | NDA021393 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2005-12-20 |
| Marketing End Date | 2017-12-07 |
| Marketing Category | NDA |
| Application Number | NDA021393 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2005-12-20 |
| Marketing End Date | 2017-12-07 |
| Marketing Category | NDA |
| Application Number | NDA021393 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2005-12-20 |
| Marketing Category | NDA |
| Application Number | NDA021393 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2005-12-20 |
| Marketing Category | NDA |
| Application Number | NDA021393 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2005-12-20 |
| Ingredient | Strength |
|---|---|
| DIPHENHYDRAMINE HYDROCHLORIDE | 25 mg/1 |
| SPL SET ID: | 405afdb4-c157-1d88-f232-848063ba4714 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| PHarm Class EPC | |
| NUI Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0573-0164 | ADVIL PM | diphenhydramine citrate and ibuprofen |
| 0573-0167 | ADVIL PM | diphenhydramine HCl, ibuprofen |
| 66715-9733 | Advil PM | Ibuprofen and Diphenhydramine citrate |
| 67751-147 | Advil PM | DIPHENHYDRAMINE CITRATE, IBUPROFEN |
| 29485-6644 | ADVIL PM- diphenhydramine citrate and ibuprofen tablet, coated | Advil PM |
| 29485-7008 | ADVIL PM- diphenhydramine citrate and ibuprofen tablet, coated | Advil PM |
| 29485-7088 | ADVIL PM- diphenhydramine citrate and ibuprofen tablet, coated | Advil PM |
| 29485-7937 | ADVIL PM- diphenhydramine citrate and ibuprofen tablet, coated | Advil PM |