Capecitabine 500mg
- Product NDC
- 72606-555
- 11-digit product format
- 726060555
- Labeler code
- 72606
- Product ID
- 72606-555_e38150f6-257d-415d-b90c-09f30f083612
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CAPECITABINE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- CELLTRION USA, INC.
- Application
- ANDA207456
- Marketing category
- ANDA
- Marketing start
- 2019-11-06
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72606-555-01 | 72606055501 | 120 TABLET, FILM COATED in 1 BOTTLE (72606-555-01) | 2019-11-06 | 0000-00-00 | No | No | Current |