Capecitabine
- Product NDC
- 42291-167
- 11-digit product format
- 422910167
- Labeler code
- 42291
- Product ID
- 42291-167_7b0b16a0-bae8-0b95-e053-2a91aa0af913
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Capecitabine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE, Inc.
- Application
- ANDA204741
- Marketing category
- ANDA
- Marketing start
- 2017-04-14
- Marketing end
- 0000-00-00
- Substance
- CAPECITABINE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record