NDC 0904-6730 – Acetaminophen
Acetaminophen 500 mg/1 · Tablet · Oral
Product NDC0904-6730
Product details
- Brand name
- Acetaminophen
- Generic name
- Acetaminophen
- Labeler
- Major Pharmaceuticals
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- OTC MONOGRAPH DRUG · M013
- Marketed since
- September 12, 2018
- Listing expires
- December 31, 2026
Active ingredients
- Acetaminophen 500 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 0904-6730-59 | 1 BOTTLE in 1 CARTON (0904-6730-59) / 100 TABLET in 1 BOTTLE | Sep 12, 2018 |
| 0904-6730-60 | 100 TABLET in 1 BOTTLE (0904-6730-60) | Sep 12, 2018 |
| 0904-6730-61 | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-6730-61) / 10 TABLET in 1 BLISTER PACK | Sep 12, 2018 |
| 0904-6730-80 | 1000 TABLET in 1 BOTTLE (0904-6730-80) | Sep 12, 2018 |
Recalls mentioning this NDC
- D-0566-2024 Jul 3, 2024 · Class II
Discoloration: Brownish tablets - D-0858-2020 Feb 19, 2020 · Class II
Presence of Foreign Tablets/Capsules: Complaint involving one Women's Prenatal dietary supplement tablet commingled in a bottle of Extra Strength Acetaminophen 500 mg contents 1000 count bottle.
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