NDC 0054-0709 – Methadone Hydrochloride
Methadone Hydrochloride 5 mg/1 · Tablet · Oral
Product NDC0054-0709
Product details
- Brand name
- Methadone Hydrochloride
- Generic name
- Methadone Hydrochloride
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA088109
- Marketed since
- March 8, 1983
- Listing expires
- December 31, 2027
- Pharmacologic class
- Opioid Agonist
Active ingredients
- Methadone Hydrochloride 5 mg/1
Uses, dosage, side effects and warnings for Methadone Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0054-0709-20 | 1 BLISTER PACK in 1 CARTON (0054-0709-20) / 100 TABLET in 1 BLISTER PACK | Mar 8, 1983 |
| 0054-0709-25 | 100 TABLET in 1 BOTTLE, PLASTIC (0054-0709-25) | Mar 8, 1983 |
Recalls mentioning this NDC
- D-0183-2025 Jan 15, 2025 · Class III
Failed Tablet/Capsule Specifications: Illegible product identification for the unit dose configuration only.
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