NDC 68180-280 – Ethambutol Hydrochloride
Ethambutol Hydrochloride 100 mg/1 · Tablet · Oral
Product NDC68180-280
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 10, 2009
- Listing expires
- December 31, 2026
- Pharmacologic class
- Antimycobacterial
Active ingredients
- Ethambutol Hydrochloride 100 mg/1
Uses, dosage, side effects and warnings for Ethambutol Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 68180-280-01 | 100 TABLET in 1 BOTTLE (68180-280-01) | Jul 10, 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.
Other Ethambutol Hydrochloride products
- 68084-280 Ethambutol Hydrochloride 400 mg/1 · Tablet · American Health Packaging
- 42806-101 Ethambutol Hydrochloride 100 mg/1 · Tablet, Film Coated · Epic Pharma, LLC
- 42806-102 Ethambutol Hydrochloride 400 mg/1 · Tablet, Film Coated · Epic Pharma, LLC
- 85742-005 Ethambutol Hydrochloride 100 mg/1 · Tablet, Film Coated · Kanchan Healthcare Inc
- 85742-006 Ethambutol Hydrochloride 400 mg/1 · Tablet, Film Coated · Kanchan Healthcare Inc
- 68180-281 Ethambutol Hydrochloride 400 mg/1 · Tablet · Lupin Pharmaceuticals, Inc.
- 10135-796 Ethambutol Hydrochloride 100 mg/1 · Tablet, Film Coated · Marlex Pharmaceuticals, Inc.
- 10135-797 Ethambutol Hydrochloride 400 mg/1 · Tablet, Film Coated · Marlex Pharmaceuticals, Inc.
- 70518-2966 Ethambutol Hydrochloride 400 mg/1 · Tablet · REMEDYREPACK INC.
- 70518-3662 Ethambutol Hydrochloride 100 mg/1 · Tablet · REMEDYREPACK INC.
- 54879-001 Ethambutol Hydrochloride 100 mg/1 · Tablet, Film Coated · STI Pharma LLC
- 54879-002 Ethambutol Hydrochloride 400 mg/1 · Tablet, Film Coated · STI Pharma LLC