NDC 59651-532 – Erlotinib
Erlotinib Hydrochloride 150 mg/1 · Tablet, Film Coated · Oral
Product NDC59651-532
Product details
- Brand name
- Erlotinib
- Generic name
- Erlotinib
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA216342
- Marketed since
- June 22, 2022
- Listing expires
- December 31, 2026
- Pharmacologic class
- Kinase Inhibitor
Active ingredients
- Erlotinib Hydrochloride 150 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 59651-532-03 | 30 TABLET, FILM COATED in 1 BOTTLE (59651-532-03) | Jun 22, 2022 |
| 59651-532-10 | 1 BLISTER PACK in 1 CARTON (59651-532-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Jun 22, 2022 |
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