NDC 0093-7662 – Erlotinib
Erlotinib Hydrochloride 25 mg/1 · Tablet, Film Coated · Oral
Product NDC0093-7662
Product details
- Brand name
- Erlotinib
- Generic name
- Erlotinib
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA091059
- Marketed since
- December 8, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- Kinase Inhibitor
Active ingredients
- Erlotinib Hydrochloride 25 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0093-7662-56 | 30 TABLET, FILM COATED in 1 BOTTLE (0093-7662-56) | Dec 8, 2021 |
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