NDC 0573-0164 – Advil Pm
Diphenhydramine Citrate 38 mg/1; Ibuprofen 200 mg/1 · Tablet, Coated · Oral
Product NDC0573-0164
Product details
- Brand name
- Advil Pm
- Generic name
- Diphenhydramine citrate and ibuprofen
- Labeler
- Haleon US Holdings LLC
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- NDA · NDA021394
- Marketed since
- December 21, 2005
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-1 Receptor Antagonist; Nonsteroidal Anti-inflammatory Drug
Active ingredients
- Diphenhydramine Citrate 38 mg/1
- Ibuprofen 200 mg/1
Package NDC codes (21)
| Package NDC | Description | Since |
|---|---|---|
| 0573-0164-04 | 4 TABLET, COATED in 1 POUCH (0573-0164-04) | Dec 21, 2005 |
| 0573-0164-05 | 2 BOTTLE in 1 CARTON (0573-0164-05) / 2 TABLET, COATED in 1 BOTTLE | Dec 21, 2005 |
| 0573-0164-08 | 1 VIAL in 1 PACKAGE (0573-0164-08) / 8 TABLET, COATED in 1 VIAL | Mar 17, 2017 |
| 0573-0164-09 | 8 TABLET, COATED in 1 VIAL (0573-0164-09) | Mar 17, 2017 |
| 0573-0164-12 | 6 POUCH in 1 CARTON (0573-0164-12) / 2 TABLET, COATED in 1 POUCH | Dec 21, 2005 |
| 0573-0164-14 | 2 POUCH in 1 CARTON (0573-0164-14) / 2 TABLET, COATED in 1 POUCH | Dec 21, 2005 |
| 0573-0164-20 | 1 BOTTLE in 1 CARTON (0573-0164-20) / 20 TABLET, COATED in 1 BOTTLE | Dec 21, 2005 |
| 0573-0164-21 | 1 BOTTLE in 1 CARTON (0573-0164-21) / 30 TABLET, COATED in 1 BOTTLE | Dec 21, 2005 |
| 0573-0164-30 | 1 BOTTLE in 1 CARTON (0573-0164-30) / 40 TABLET, COATED in 1 BOTTLE | Dec 21, 2005 |
| 0573-0164-32 | 1 BOTTLE in 1 CARTON (0573-0164-32) / 50 TABLET, COATED in 1 BOTTLE | Dec 21, 2005 |
| 0573-0164-33 | 1 BOTTLE in 1 CARTON (0573-0164-33) / 50 TABLET, COATED in 1 BOTTLE | Dec 21, 2005 |
| 0573-0164-40 | 1 BOTTLE in 1 CARTON (0573-0164-40) / 80 TABLET, COATED in 1 BOTTLE | Dec 21, 2005 |
| 0573-0164-41 | 1 BOTTLE in 1 CARTON (0573-0164-41) / 100 TABLET, COATED in 1 BOTTLE | Dec 21, 2005 |
| 0573-0164-43 | 1 BOTTLE in 1 CARTON (0573-0164-43) / 120 TABLET, COATED in 1 BOTTLE | Dec 21, 2005 |
| 0573-0164-44 | 1 BOTTLE in 1 CARTON (0573-0164-44) / 140 TABLET, COATED in 1 BOTTLE | Dec 21, 2005 |
| 0573-0164-45 | 1 BOTTLE in 1 CARTON (0573-0164-45) / 180 TABLET, COATED in 1 BOTTLE | Dec 21, 2005 |
| 0573-0164-46 | 1 BOTTLE in 1 CARTON (0573-0164-46) / 180 TABLET, COATED in 1 BOTTLE | Dec 21, 2005 |
| 0573-0164-49 | 1 BOTTLE in 1 CARTON (0573-0164-49) / 200 TABLET, COATED in 1 BOTTLE | Dec 21, 2005 |
| 0573-0164-55 | 50 POUCH in 1 TRAY (0573-0164-55) / 2 TABLET, COATED in 1 POUCH | Dec 21, 2005 |
| 0573-0164-65 | 120 TABLET, COATED in 1 BOTTLE (0573-0164-65) | Sep 30, 2016 |
| 0573-0164-91 | 3000 POUCH in 1 BOX (0573-0164-91) / 2 TABLET, COATED in 1 POUCH | Dec 21, 2005 |
Recalls mentioning this NDC
- D-1166-2014 Mar 26, 2014 · Class III
Subpotent Drug: This lot is being recalled because of out-of-specification test results for Diphenhydramine citrate.
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- 0573-0148 Diphenhydramine Hydrochloride 25 mg/1; Ibuprofen 200 mg/1 · Capsule, Liquid Filled · Haleon US Holdings LLC
- 0573-0167 Diphenhydramine Hydrochloride 25 mg/1; Ibuprofen 200 mg/1 · Capsule, Liquid Filled · Haleon US Holdings LLC