NDC 0363-0050 – Ibuprofen PM
Diphenhydramine Citrate 38 mg/1; Ibuprofen 200 mg/1 · Tablet, Film Coated · Oral
Product NDC0363-0050
Product details
- Brand name
- Ibuprofen PM
- Generic name
- Diphenhydramine citrate, ibuprofen
- Labeler
- Walgreen Company
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA079113
- Marketed since
- February 19, 2009
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 0363-0050-27 | 1 BOTTLE in 1 CARTON (0363-0050-27) / 80 TABLET, FILM COATED in 1 BOTTLE | Feb 19, 2009 |
| 0363-0050-58 | 1 BOTTLE in 1 CARTON (0363-0050-58) / 40 TABLET, FILM COATED in 1 BOTTLE | Jul 12, 2013 |
| 0363-0050-60 | 1 BOTTLE in 1 CARTON (0363-0050-60) / 20 TABLET, FILM COATED in 1 BOTTLE | Feb 19, 2009 |
| 0363-0050-76 | 1 BOTTLE in 1 CARTON (0363-0050-76) / 120 TABLET, FILM COATED in 1 BOTTLE | Jan 7, 2016 |
| 0363-0050-82 | 200 TABLET, FILM COATED in 1 BOTTLE (0363-0050-82) | Sep 21, 2017 |
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