NDC 50844-235 – Pain Reliever PM Extra Strength
Acetaminophen 500 mg/1; Diphenhydramine Hydrochloride 25 mg/1 · Tablet, Film Coated · Oral
Product NDC50844-235
Product details
- Brand name
- Pain Reliever PM Extra Strength
- Generic name
- Acetaminophen, Diphenhydramine HCl
- Labeler
- L.N.K. International, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- OTC MONOGRAPH DRUG · M013
- Marketed since
- May 15, 1994
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
- Acetaminophen 500 mg/1
- Diphenhydramine Hydrochloride 25 mg/1
Uses, dosage, side effects and warnings for Pain Reliever PM →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 50844-235-15 | 1 BOTTLE, PLASTIC in 1 CARTON (50844-235-15) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | May 15, 1994 |
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