NDC 63941-095 – Extra Strength Pain Relief PM
Acetaminophen 500 mg/1; Diphenhydramine Hydrochloride 25 mg/1 · Tablet, Coated · Oral
Product NDC63941-095
Product details
- Brand name
- Extra Strength Pain Relief PM
- Generic name
- Acetaminophen and Diphenhydramine Hydrochloride
- Labeler
- VALU MERCHANDISERS COMPANY
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- OTC MONOGRAPH DRUG · M013
- Marketed since
- February 1, 2010
- Marketing end
- March 31, 2028
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
- Acetaminophen 500 mg/1
- Diphenhydramine Hydrochloride 25 mg/1
Uses, dosage, side effects and warnings for Extra Strength Pain Relief PM →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 63941-095-02 | 1 BOTTLE, PLASTIC in 1 CARTON (63941-095-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC | Feb 1, 2010 |
| 63941-095-03 | 1 BOTTLE, PLASTIC in 1 CARTON (63941-095-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC | Oct 4, 2011 |
| 63941-095-09 | 2 BOTTLE, PLASTIC in 1 CARTON (63941-095-09) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC | Feb 3, 2012 |