NDC 21130-814 – Naproxen Sodium Diphenhydramine Hydrochloride
Naproxen Sodium 220 mg/1; Diphenhydramine Hydrochloride 25 mg/1 · Tablet · Oral
Product NDC21130-814
Product details
- Brand name
- Naproxen Sodium Diphenhydramine Hydrochloride
- Generic name
- Naproxen Sodium Diphenhydramine Hydrochloride
- Labeler
- SAFEWAY
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA213663
- Marketed since
- June 30, 2023
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-1 Receptor Antagonist; Nonsteroidal Anti-inflammatory Drug
Active ingredients
- Naproxen Sodium 220 mg/1
- Diphenhydramine Hydrochloride 25 mg/1
Uses, dosage, side effects and warnings for Naproxen Sodium Diphenhydramine Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 21130-814-05 | 50 TABLET in 1 BOTTLE (21130-814-05) | Jun 30, 2023 |