NDC 68180-281 – Ethambutol Hydrochloride
Ethambutol Hydrochloride 400 mg/1 · Tablet · Oral
Product NDC68180-281
Product details
- Brand name
- Ethambutol Hydrochloride
- Generic name
- Ethambutol Hydrochloride
- Labeler
- Lupin Pharmaceuticals, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078939
- Marketed since
- July 4, 2009
- Listing expires
- December 31, 2026
- Pharmacologic class
- Antimycobacterial
Active ingredients
- Ethambutol Hydrochloride 400 mg/1
Uses, dosage, side effects and warnings for Ethambutol Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 68180-281-01 | 100 TABLET in 1 BOTTLE (68180-281-01) | Jul 4, 2009 |
Recalls mentioning this NDC
- D-346-2014 Dec 18, 2013 · Class III
Failed Impurities/Degradation Specifications: This product is being recalled due to an out of specification result for an impurity.
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