Erlotinib 100 mg / 1 Tablet 30 Tablet, Film Coated

Reference details for licensed healthcare facility review and verification.

NDC 1163304-0096-30
Product NDC63304-0096
Generic Drug NameErlotinib
Brand NameErlotinib
ManufacturerSun Pharmaceutical Industries, Inc.
Strength100 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity30 Tablet, Film Coated
Package Description30 TABLET, FILM COATED in 1 BOTTLE (63304-096-30)
Active IngredientsErlotinib
Marketing CategoryANDA

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NDC snapshot

Erlotinib 100 mg / 1 Tablet is tracked under NDC 63304-0096-30 and rolls up into product family 63304-0096. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 30 Tablet, Film Coated.
  • Manufacturer: Sun Pharmaceutical Industries, Inc..
  • Dosage form: Tablet.
  • Family size: 2 indexed presentations.

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Official references

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Alternate presentations in this family

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Potential alternatives with matching presentation

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View Potential Alternative HubErlotinib 100 mg / 1 Tablet 30 Tablet, Film Coated Bottle4 package-level listings in the comparison hub.

Sample package-level pages in this comparison set

Erlotinib 100 mg / 1 Tablet 30 Tablet, Film Coated, NDC 63304-0096-30, is a Sun Pharmaceutical Industries, Inc. 100 mg / 1 tablet presentation packaged as 30 Tablet, Film Coated.

NDC search formats

  • Canonical NDC 11: 63304-0096-30
  • Digits-only NDC 11: 63304009630
  • Possible 10-digit display format: 63304-096-30 (6330409630)

Helpful product links

  • Search by brand name: Erlotinib
  • NDC 11: 63304-0096-30
  • Product family NDC: 63304-0096
  • Other package sizes in this family: 3 Blister Pack
  • Compare related presentations: Erlotinib 100 mg / 1 Tablet 3 Blister Pack
  • VA classification code: AN900
  • VA classification code description: ANTINEOPLASTIC,OTHER
  • CMOP ID: E0401
  • VUID: 4017406