72205-082 : Erlotinib Hydrochloride 150 mg Oral Tablet, Film Coated
NDC: | 72205-082 |
Labeler: | Novadoz Pharmaceuticals LLC |
Product Type: | Human Prescription Drug |
Drug Name: | Erlotinib Hydrochloride |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | ANDA214366 |
Rev. Date: |
NDC Package Codes:
- 72205-082-30: 1 BOTTLE IN 1 CARTON (72205‑082‑30) > 30 TABLET, FILM COATED IN 1 BOTTLE
Active Ingredients:
- Erlotinib Hydrochloride
Dosage Strength:
- 150 mg
Pharmaceutical Classes:
- Kinase Inhibitor [EPC]
- Protein Kinase Inhibitors [MoA]
Related Products:
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- 42292-051 Erlotinib Hydrochloride Hydrochloride 25 mg Oral Tablet, Film Coated by Mylan Institutional Inc.
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- 42292-053 Erlotinib Hydrochloride Hydrochloride 150 mg Oral Tablet, Film Coated by Mylan Institutional Inc.
- 46708-565 Erlotinib Hydrochloride 25 mg Oral Tablet, Film Coated by Alembic Pharmaceuticals Limited
- 46708-566 Erlotinib Hydrochloride 100 mg Oral Tablet, Film Coated by Alembic Pharmaceuticals Limited
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- 62332-565 Erlotinib Hydrochloride 25 mg Oral Tablet, Film Coated by Alembic Pharmaceuticals Inc.
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- 62332-567 Erlotinib Hydrochloride 150 mg Oral Tablet, Film Coated by Alembic Pharmaceuticals Inc.
- 69539-090 Erlotinib Hydrochloride 25 mg Oral Tablet, Film Coated by Msn Laboratories Private Limited
- 69539-091 Erlotinib Hydrochloride 100 mg Oral Tablet, Film Coated by Msn Laboratories Private Limited
- 69539-092 Erlotinib Hydrochloride 150 mg Oral Tablet, Film Coated by Msn Laboratories Private Limited
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.