NDC 63304-135 – Erlotinib
Erlotinib 150 mg/1 · Tablet, Film Coated · Oral
Product NDC63304-135
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 150 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 63304-135-11 | 3 BLISTER PACK in 1 CARTON (63304-135-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK (63304-135-31) | Nov 5, 2019 |
| 63304-135-30 | 30 TABLET, FILM COATED in 1 BOTTLE (63304-135-30) | Nov 5, 2019 |
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