Erlotinib 150 mg / 1 Tablet 30 Tablet, Film Coated
Comprehensive product details for sourcing and verification.
| NDC 11 | 00093-7664-56 |
|---|---|
| Product NDC | 00093-7664 |
| Generic Drug Name | Erlotinib |
| Brand Name | Erlotinib |
| Manufacturer | Teva Pharmaceuticals USA, Inc. |
| Strength | 150 mg / 1 |
| Dosage Form | Tablet |
| Drug Type | Oral |
| Package Quantity | 30 Tablet, Film Coated |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (0093-7664-56) |
| Active Ingredients | Erlotinib Hydrochloride |
| Marketing Category | ANDA |
Unless explicitly stated in writing, no direct affiliation, sponsorship, or endorsement by individual product manufacturers with Premium Rx National, LLC should be implied. All brand names, trade names, and trademarks are the property of their respective owners and are presented solely for accurate product identification and informational reference.
NDC snapshot
Erlotinib 150 mg / 1 Tablet is tracked under NDC 00093-7664-56 and rolls up into product family 00093-7664. Use this page to confirm the exact presentation before moving into related family or manufacturer pathways.
- Package configuration: 30 Tablet, Film Coated.
- Manufacturer: Teva Pharmaceuticals USA, Inc..
- Dosage form: Tablet.
- Family size: 1 active presentation.
Click a tag to refine the catalog view around this exact presentation.
Official references
Use official labeling and directory references to confirm presentation details while your team reviews the PRN catalog entry and related sourcing paths.
Erlotinib 150 mg / 1 Tablet 30 Tablet, Film Coated, NDC 00093-7664-56, is a Teva Pharmaceuticals USA, Inc. 150 mg / 1 tablet presentation packaged as 30 Tablet, Film Coated.
NDC search formats
- Canonical NDC 11: 00093-7664-56.
- Digits-only NDC 11: 00093766456.
- Possible 10-digit display format: 0093-7664-56 (0093766456).
Helpful product links
- Search by brand name: Erlotinib.
- Exact NDC 11: 00093-7664-56.
- Product family NDC: 00093-7664.