ANASTROZOLE
- Product NDC
- 76519-1224
- 11-digit product format
- 765191224
- Labeler code
- 76519
- Product ID
- 76519-1224_8270c509-4c1d-bfd8-e053-2991aa0abb90
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ANASTROZOLE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- H.J. Harkins Company, Inc.
- Application
- ANDA090568
- Marketing category
- ANDA
- Marketing start
- 2019-02-15
- 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
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76519-1224-3 | ANASTROZOLE | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76519-1224 | ANASTROZOLE TABLET [H.J. HARKINS COMPANY, INC.] | 1 | Legacy NDC, 1 package rows | 20190308_8270c509-4c1c-bfd8-e053-2991aa0abb90.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 76519-1224-3 | 76519122403 | 30 TABLET in 1 BOTTLE (76519-1224-3) | 30 tablet | 2019-02-15 | 0000-00-00 | No | No | Current |