Anastrozole
- Product NDC
- 62175-710
- 11-digit product format
- 621750710
- Labeler code
- 62175
- Product ID
- 62175-710_06ce076b-eee1-42cf-b9f6-f5608c0a656f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Anastrozole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lannett Company, Inc..
- Application
- ANDA091331
- Marketing category
- ANDA
- Marketing start
- 2011-01-05
- Marketing end
- 0000-00-00
- Substance
- ANASTROZOLE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Aromatase Inhibitor [EPC],Aromatase Inhibitors [MoA]
- 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 |
|---|
| 62175-710-32 | 62175071032 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (62175-710-32) | 2011-01-05 | 0000-00-00 | No | No | Current |