NDC 31722-264 – Erlotinib
Erlotinib Hydrochloride 100 mg/1 · Tablet, Film Coated · Oral
Product NDC31722-264
Product details
- Brand name
- Erlotinib
- Generic name
- Erlotinib
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA209267
- Marketed since
- May 24, 2024
- Listing expires
- December 31, 2026
- Pharmacologic class
- Kinase Inhibitor
Active ingredients
- Erlotinib Hydrochloride 100 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 31722-264-30 | 1 BOTTLE in 1 CARTON (31722-264-30) / 30 TABLET, FILM COATED in 1 BOTTLE | May 24, 2024 |
Other Erlotinib products
- 72485-219 Erlotinib Hydrochloride 150 mg/1 · Tablet, Film Coated · Armas Pharmaceuticals Inc.
- 72485-218 Erlotinib Hydrochloride 100 mg/1 · Tablet, Film Coated · Armas Pharmaceuticals Inc.
- 72485-217 Erlotinib Hydrochloride 25 mg/1 · Tablet, Film Coated · Armas Pharmaceuticals Inc.
- 59651-530 Erlotinib Hydrochloride 25 mg/1 · Tablet, Film Coated · Aurobindo Pharma Limited
- 59651-531 Erlotinib Hydrochloride 100 mg/1 · Tablet, Film Coated · Aurobindo Pharma Limited
- 59651-532 Erlotinib Hydrochloride 150 mg/1 · Tablet, Film Coated · Aurobindo Pharma Limited
- 31722-263 Erlotinib Hydrochloride 25 mg/1 · Tablet, Film Coated · Camber Pharmaceuticals, Inc.
- 31722-265 Erlotinib Hydrochloride 150 mg/1 · Tablet, Film Coated · Camber Pharmaceuticals, Inc.
- 63304-135 Erlotinib 150 mg/1 · Tablet, Film Coated · Sun Pharmaceutical Industries, Inc.
- 63304-096 Erlotinib 100 mg/1 · Tablet, Film Coated · Sun Pharmaceutical Industries, Inc.
- 63304-095 Erlotinib 25 mg/1 · Tablet, Film Coated · Sun Pharmaceutical Industries, Inc.
- 0093-7662 Erlotinib Hydrochloride 25 mg/1 · Tablet, Film Coated · Teva Pharmaceuticals USA, Inc.