Erlotinib Hydrochloride 100 mg / 1 Tablet 1 Bottle
Reference details for licensed healthcare facility review and verification.
| NDC 11 | 72205-0081-30 |
|---|---|
| Product NDC | 72205-0081 |
| Generic Drug Name | Erlotinib Hydrochloride |
| Brand Name | Erlotinib Hydrochloride |
| Manufacturer | Novadoz Pharmaceuticals LLC |
| Strength | 100 mg / 1 |
| Dosage Form | Tablet |
| Drug Type | Oral |
| Package Quantity | 1 Bottle |
| Package Description | 1 BOTTLE in 1 CARTON (72205-081-30) / 30 TABLET, FILM COATED in 1 BOTTLE |
| Active Ingredients | Erlotinib Hydrochloride |
| Marketing Category | ANDA |
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NDC snapshot
Erlotinib Hydrochloride 100 mg / 1 Tablet is tracked under NDC 72205-0081-30 and rolls up into product family 72205-0081. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.
- Package configuration: 1 Bottle.
- Manufacturer: Novadoz Pharmaceuticals LLC.
- Dosage form: Tablet.
- Family size: 1 indexed presentation.
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Official references
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Potential alternatives with matching presentation
Open the comparison hub or review package-level listings from 2 product-NDC families with matching normalized presentation details. Review each product detail page before treating any item as a true alternative.
Erlotinib Hydrochloride 100 mg / 1 Tablet 1 Bottle, NDC 72205-0081-30, is a Novadoz Pharmaceuticals LLC 100 mg / 1 tablet presentation packaged as 1 Bottle.
NDC search formats
- Canonical NDC 11: 72205-0081-30
- Digits-only NDC 11: 72205008130
- Possible 10-digit display format: 72205-081-30 (7220508130)
Helpful product links
- Search by brand name: Erlotinib Hydrochloride
- NDC 11: 72205-0081-30
- Product family NDC: 72205-0081
- VA classification code: AN900
- VA classification code description: ANTINEOPLASTIC,OTHER
- CMOP ID: E0401
- VUID: 4017406