NDC 72485-218 – Erlotinib
Erlotinib Hydrochloride 100 mg/1 · Tablet, Film Coated · Oral
Product NDC72485-218
Product details
- Brand name
- Erlotinib
- Generic name
- Erlotinib hydrochloride
- Labeler
- Armas Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA211960
- Marketed since
- November 6, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Kinase Inhibitor
Active ingredients
- Erlotinib Hydrochloride 100 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 72485-218-30 | 1 BOTTLE in 1 BOX (72485-218-30) / 30 TABLET, FILM COATED in 1 BOTTLE | Nov 6, 2019 |
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