Anastrozole
- Product NDC
- 50090-5812
- 11-digit product format
- 500905812
- Labeler code
- 50090
- Product ID
- 50090-5812_647aef71-6a73-402a-bdb1-335ddf95e136
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Anastrozole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA212434
- Marketing category
- ANDA
- Marketing start
- 2020-07-24
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5812-0 | 50090581200 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-5812-0) | 2021-10-18 | 0000-00-00 | No | No | Current |
| 50090-5812-1 | 50090581201 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-5812-1) | 2021-10-18 | 0000-00-00 | No | No | Current |