Anastrozole
- Product NDC
- 70518-2484
- 11-digit product format
- 705182484
- Labeler code
- 70518
- Product ID
- 70518-2484_d0ff4dac-d820-256b-e053-2995a90ad53c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Anastrozole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090568
- Marketing category
- ANDA
- Marketing start
- 2019-12-13
- 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#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2484 | ANASTROZOLE TABLET [REMEDYREPACK INC.] | 7 | Legacy NDC | 20250116_5e9d46e6-e6e3-4dd0-9bf5-dbfa2fdd2ce3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2484-0 | 70518248400 | 30 POUCH in 1 BOX (70518-2484-0) > 1 TABLET in 1 POUCH (70518-2484-1) | 30 pouch | 2019-12-13 | 0000-00-00 | No | No | Current |