Anastrozole
- Product NDC
- 68788-6774
- 11-digit product format
- 687886774
- Labeler code
- 68788
- Product ID
- 68788-6774_5b8246b5-94ca-4304-8297-233422677e59
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Anastrozole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA090568
- Marketing category
- ANDA
- Marketing start
- 2016-10-24
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-6774-3 | 68788677403 | 30 TABLET in 1 BOTTLE, PLASTIC (68788-6774-3) | 30 tablet | 2016-10-24 | 0000-00-00 | No | No | Current |
| 68788-6774-6 | 68788677406 | 60 TABLET in 1 BOTTLE, PLASTIC (68788-6774-6) | 60 tablet | 2016-10-24 | 0000-00-00 | No | No | Current |
| 68788-6774-9 | 68788677409 | 90 TABLET in 1 BOTTLE, PLASTIC (68788-6774-9) | 90 tablet | 2016-10-24 | 0000-00-00 | No | No | Current |