Drug
Erlotinib NDC Codes
Erlotinib is listed in the FDA NDC Directory as 21 finished products from 7 labelers.
Overview
Active ingredients: Erlotinib hydrochloride, Erlotinib. Each product below links to its own NDC page with package NDCs in 10- and 11-digit form.
- Generic name
- Erlotinib; Erlotinib hydrochloride
- Active ingredients
- Erlotinib hydrochloride, Erlotinib
- Labelers
- Camber Pharmaceuticals, Inc., Aurobindo Pharma Limited, Teva Pharmaceuticals USA, Inc., Zydus Lifesciences Limited, Zydus Pharmaceuticals USA Inc., Armas Pharmaceuticals Inc., Sun Pharmaceutical Industries, Inc.
- Strengths
- Erlotinib hydrochloride 25 mg/1; Erlotinib hydrochloride 100 mg/1; Erlotinib hydrochloride 150 mg/1; Erlotinib 25 mg/1; Erlotinib 100 mg/1; Erlotinib 150 mg/1
- Dosage forms
- Tablet, Film coated, Tablet
- Routes
- Oral
- Drug classes (FDA established)
- Kinase Inhibitor
- HCPCS / J-code
- None in Med-Code's directory for these products
- Package NDCs
- 39
NDC codes
Newest listings first. Each row links to the product’s NDC page.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) | HCPCS |
|---|---|---|---|---|---|---|
| Erlotinib | Erlotinib hydrochloride 25 mg/1 | Tablet, Film coatedOral | Camber Pharmaceuticals, Inc. | 31722-263 | 31722-0263-30 | — |
| Erlotinib | Erlotinib hydrochloride 100 mg/1 | Tablet, Film coatedOral | Camber Pharmaceuticals, Inc. | 31722-264 | 31722-0264-30 | — |
| Erlotinib | Erlotinib hydrochloride 150 mg/1 | Tablet, Film coatedOral | Camber Pharmaceuticals, Inc. | 31722-265 | 31722-0265-30 | — |
| Erlotinib | Erlotinib hydrochloride 25 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 59651-530 | 59651-0530-0359651-0530-10 | — |
| Erlotinib | Erlotinib hydrochloride 100 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 59651-531 | 59651-0531-0359651-0531-10 | — |
| Erlotinib | Erlotinib hydrochloride 150 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 59651-532 | 59651-0532-0359651-0532-10 | — |
| Erlotinib | Erlotinib hydrochloride 25 mg/1 | Tablet, Film coatedOral | Teva Pharmaceuticals USA, Inc. | 0093-7662 | 00093-7662-56 | — |
| Erlotinib | Erlotinib hydrochloride 25 mg/1 | Tablet, Film coatedOral | Zydus Lifesciences Limited | 70771-1521 | 70771-1521-0370771-1521-0770771-1521-09 | — |
| Erlotinib | Erlotinib hydrochloride 100 mg/1 | Tablet, Film coatedOral | Zydus Lifesciences Limited | 70771-1522 | 70771-1522-0370771-1522-0770771-1522-09 | — |
| Erlotinib | Erlotinib hydrochloride 150 mg/1 | Tablet, Film coatedOral | Zydus Lifesciences Limited | 70771-1523 | 70771-1523-0370771-1523-0770771-1523-09 | — |
| Erlotinib | Erlotinib hydrochloride 25 mg/1 | TabletOral | Zydus Pharmaceuticals USA Inc. | 68382-913 | 68382-0913-0668382-0913-1668382-0913-84 | — |
| Erlotinib | Erlotinib hydrochloride 100 mg/1 | TabletOral | Zydus Pharmaceuticals USA Inc. | 68382-914 | 68382-0914-0668382-0914-1668382-0914-84 | — |
| Erlotinib | Erlotinib hydrochloride 150 mg/1 | TabletOral | Zydus Pharmaceuticals USA Inc. | 68382-915 | 68382-0915-0668382-0915-1668382-0915-84 | — |
| Erlotiniberlotinib hydrochloride | Erlotinib hydrochloride 25 mg/1 | Tablet, Film coatedOral | Armas Pharmaceuticals Inc. | 72485-217 | 72485-0217-30 | — |
| Erlotiniberlotinib hydrochloride | Erlotinib hydrochloride 100 mg/1 | Tablet, Film coatedOral | Armas Pharmaceuticals Inc. | 72485-218 | 72485-0218-30 | — |
| Erlotiniberlotinib hydrochloride | Erlotinib hydrochloride 150 mg/1 | Tablet, Film coatedOral | Armas Pharmaceuticals Inc. | 72485-219 | 72485-0219-30 | — |
| Erlotinib | Erlotinib 25 mg/1 | Tablet, Film coatedOral | Sun Pharmaceutical Industries, Inc. | 63304-095 | 63304-0095-1163304-0095-30 | — |
| Erlotinib | Erlotinib 100 mg/1 | Tablet, Film coatedOral | Sun Pharmaceutical Industries, Inc. | 63304-096 | 63304-0096-1163304-0096-30 | — |
| Erlotinib | Erlotinib 150 mg/1 | Tablet, Film coatedOral | Sun Pharmaceutical Industries, Inc. | 63304-135 | 63304-0135-1163304-0135-30 | — |
| Erlotinib | Erlotinib hydrochloride 100 mg/1 | Tablet, Film coatedOral | Teva Pharmaceuticals USA, Inc. | 0093-7663 | 00093-7663-56 | — |
| Erlotinib | Erlotinib hydrochloride 150 mg/1 | Tablet, Film coatedOral | Teva Pharmaceuticals USA, Inc. | 0093-7664 | 00093-7664-56 | — |
Erlotinib: common questions
- What is the NDC for Erlotinib?
- Erlotinib has 21 product NDCs, one for each strength, dosage form and labeler; each product NDC then has one package NDC per package size. Pick the row for your product above to see its package NDCs.
- Is there a J-code for Erlotinib?
- Med-Code's curated HCPCS directory has no drug-specific code for these products. Drugs dispensed by a pharmacy are billed by NDC. NDC vs J-code.
- Which NDC goes on a claim?
- The package NDC of what was given, in 11-digit form. How to convert a 10-digit NDC.