NDC 68382-042 – Promethazine Hydrochloride
Promethazine Hydrochloride 50 mg/1 · Tablet · Oral
Product NDC68382-042
Product details
- Brand name
- Promethazine Hydrochloride
- Generic name
- Promethazine Hydrochloride
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA040596
- Marketed since
- December 14, 2005
- Listing expires
- December 31, 2026
- Pharmacologic class
- Phenothiazine
Active ingredients
- Promethazine Hydrochloride 50 mg/1
Uses, dosage, side effects and warnings for Promethazine Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68382-042-01 | 100 TABLET in 1 BOTTLE (68382-042-01) | Dec 14, 2005 |
| 68382-042-05 | 500 TABLET in 1 BOTTLE (68382-042-05) | Dec 14, 2005 |
| 68382-042-10 | 1000 TABLET in 1 BOTTLE (68382-042-10) | Dec 14, 2005 |
Recalls mentioning this NDC
- D-1342-2014 May 28, 2014 · Class II
Presence of Foreign Tablets: Presence of atenolol 25 mg tablet mixed into promethazine 25 mg tablet bottles.
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