NDC 63304-096 – Erlotinib
Erlotinib 100 mg/1 · Tablet, Film Coated · Oral
Product NDC63304-096
Product details
- Brand name
- Erlotinib
- Generic name
- Erlotinib
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA210300
- Marketed since
- November 5, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Kinase Inhibitor
Active ingredients
- Erlotinib 100 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 63304-096-11 | 3 BLISTER PACK in 1 CARTON (63304-096-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK (63304-096-31) | Nov 5, 2019 |
| 63304-096-30 | 30 TABLET, FILM COATED in 1 BOTTLE (63304-096-30) | Nov 5, 2019 |
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.
- 31722-264 Erlotinib Hydrochloride 100 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.
- 63304-095 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.