NDC 0067-2200 – Excedrin Rapid Relief
Acetaminophen 500 mg/1 · Tablet · Oral
Product NDC0067-2200
Product details
- Brand name
- Excedrin Rapid Relief
- Generic name
- Acetaminophen
- Labeler
- Haleon US Holdings LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- OTC MONOGRAPH DRUG · M013
- Marketed since
- March 31, 2026
- Listing expires
- December 31, 2027
Active ingredients
- Acetaminophen 500 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 0067-2200-20 | 1 BOTTLE in 1 CARTON (0067-2200-20) / 20 TABLET in 1 BOTTLE | Mar 31, 2026 |
| 0067-2200-80 | 1 BOTTLE in 1 CARTON (0067-2200-80) / 80 TABLET in 1 BOTTLE | Mar 31, 2026 |
| 0067-2200-82 | 1 BOTTLE in 1 CARTON (0067-2200-82) / 160 TABLET in 1 BOTTLE | Mar 31, 2026 |
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- 0067-8139 Acetaminophen 500 mg/1; Caffeine 65 mg/1 · Tablet, Film Coated · Haleon US Holdings LLC
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- 0067-2040 Acetaminophen 250 mg/1; Aspirin 250 mg/1; Caffeine 65 mg/1 · Tablet, Film Coated · Haleon US Holdings LLC
- 0067-2039 Acetaminophen 250 mg/1; Aspirin 250 mg/1; Caffeine 65 mg/1 · Tablet, Film Coated · Haleon US Holdings LLC
- 0067-2035 Acetaminophen 250 mg/1; Aspirin 250 mg/1; Caffeine 65 mg/1 · Tablet, Coated · Haleon US Holdings LLC
- 0067-2021 Acetaminophen 250 mg/1; Aspirin 250 mg/1; Caffeine 65 mg/1 · Tablet, Coated · Haleon US Holdings LLC
- 0067-2003 Acetaminophen 250 mg/1; Aspirin 250 mg/1; Caffeine 65 mg/1 · Tablet, Film Coated · Haleon US Holdings LLC