NDC 46708-565 – Erlotinib Hydrochloride
Erlotinib Hydrochloride 25 mg/1 · Tablet, Film Coated · Oral
Product NDC46708-565
Product details
- Brand name
- Erlotinib Hydrochloride
- Generic name
- Erlotinib Hydrochloride
- Labeler
- Alembic Pharmaceuticals Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA214719
- Marketed since
- July 9, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- Kinase Inhibitor
Active ingredients
- Erlotinib Hydrochloride 25 mg/1
Uses, dosage, side effects and warnings for Erlotinib Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 46708-565-30 | 30 TABLET, FILM COATED in 1 BOTTLE (46708-565-30) | Jul 9, 2021 |
| 46708-565-90 | 90 TABLET, FILM COATED in 1 BOTTLE (46708-565-90) | Jul 9, 2021 |
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