NDC 68001-495 – Acetaminophen
Acetaminophen 650 mg/1 · Tablet · Oral
Product NDC68001-495
Product details
- Brand name
- Acetaminophen
- Generic name
- Acetaminophen
- Labeler
- BluePoint Laboratories
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA207229
- Marketed since
- April 30, 2021
- Listing expires
- December 31, 2026
Active ingredients
- Acetaminophen 650 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 68001-495-00 | 1 BOTTLE in 1 CARTON (68001-495-00) / 100 TABLET in 1 BOTTLE | Apr 30, 2021 |
Other Acetaminophen products
- 50090-0001 Acetaminophen 120 mg/1 · Suppository · A-S Medication Solutions
- 50090-5272 Acetaminophen 500 mg/1 · Tablet · A-S Medication Solutions
- 50090-5313 Acetaminophen 500 mg/1 · Tablet · A-S Medication Solutions
- 50090-6059 Acetaminophen 160 mg/5mL · Liquid · A-S Medication Solutions
- 50090-5350 Acetaminophen 500 mg/1 · Tablet · A-S Medication Solutions
- 57344-004 Acetaminophen 500 mg/1 · Tablet, Coated · AAA Pharmaceutical, Inc.
- 82568-0002 Acetaminophen 500 mg/1 · Tablet · AARNA USA INC.
- 82568-0001 Acetaminophen 325 mg/1 · Tablet · AARNA USA INC.
- 52343-555 Acetaminophen 160 mg/5mL · Solution · Acetris Pharma Holdings, LLC
- 17714-012 Acetaminophen 325 mg/1 · Tablet · Advance Pharmaceutical Inc.
- 71399-1025 Acetaminophen 325 mg/1 · Tablet · Akron Pharma Inc.
- 71399-1026 Acetaminophen 500 mg/1 · Tablet · Akron Pharma Inc.