NDC 37808-264 – Naproxen sodium pm
Diphenhydramine Hydrochloride 25 mg/1; Naproxen Sodium 220 mg/1 · Tablet, Film Coated · Oral
Product NDC37808-264
Product details
- Brand name
- Naproxen sodium pm
- Generic name
- Diphenhydramine hydrochloride, naproxen sodium
- Labeler
- H E B
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208499
- Marketed since
- October 13, 2020
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-1 Receptor Antagonist; Nonsteroidal Anti-inflammatory Drug
Active ingredients
- Diphenhydramine Hydrochloride 25 mg/1
- Naproxen Sodium 220 mg/1
Uses, dosage, side effects and warnings for Naproxen Sodium PM →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 37808-264-27 | 1 BOTTLE in 1 CARTON (37808-264-27) / 80 TABLET, FILM COATED in 1 BOTTLE | Oct 13, 2020 |
| 37808-264-60 | 1 BOTTLE in 1 CARTON (37808-264-60) / 20 TABLET, FILM COATED in 1 BOTTLE | Oct 13, 2020 |
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