Anastrozole
- Product NDC
- 21695-990
- 11-digit product format
- 216950990
- Labeler code
- 21695
- Product ID
- 21695-990_611e1f43-1442-4cbb-b7eb-b65de15c6c70
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Anastrozole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- ANDA079220
- Marketing category
- ANDA
- Marketing start
- 2010-07-01
- Marketing end
- 0000-00-00
- Substance
- ANASTROZOLE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Aromatase Inhibitor [EPC],Aromatase Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 9495fd23-86bb-d8f7-ae78-6dfe2f4dae2d | Product name | 3 | 20210204 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 21695-990-30 | 2019-09-24 | C162847 | 48780-1 | 934fe258-4c35-48b1-e053-8cdaa90a720a | HIGHLIGHTS OF PRESCRIBING INFORMATION These highlights do not include all the information needed to use anastrozole tablets safely and effectively. See full prescribing information for anastrozole tablets. Initial U.S. Approval: |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 21695-990-30 | Anastrozole | 30 in 1 BOTTLE | TABLET | 30 | 1 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 21695-990-30 | EA - Each | 21695-990 | 2313f3be-e125-4a75-b610-475f04dd975e | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| ANASTROZOLE | ACTIVE INGREDIENT | 2Z07MYW1AZ | ANASTROZOLE TABLET [REBEL DISTRIBUTORS CORP] | 1 | |
| ANASTROZOLE | ACTIVE MOIETY | 2Z07MYW1AZ | ANASTROZOLE TABLET [REBEL DISTRIBUTORS CORP] | 1 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | ANASTROZOLE TABLET [REBEL DISTRIBUTORS CORP] | 1 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | ANASTROZOLE TABLET [REBEL DISTRIBUTORS CORP] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | ANASTROZOLE TABLET [REBEL DISTRIBUTORS CORP] | 1 | |
| POLYETHYLENE GLYCOL | INACTIVE INGREDIENT | 3WJQ0SDW1A | ANASTROZOLE TABLET [REBEL DISTRIBUTORS CORP] | 1 | |
| POVIDONE K30 | INACTIVE INGREDIENT | U725QWY32X | ANASTROZOLE TABLET [REBEL DISTRIBUTORS CORP] | 1 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | ANASTROZOLE TABLET [REBEL DISTRIBUTORS CORP] | 1 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | ANASTROZOLE TABLET [REBEL DISTRIBUTORS CORP] | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 199224 | anastrozole 1 MG Oral Tablet | PSN | 611e1f43-1442-4cbb-b7eb-b65de15c6c70 | 1 |
| 199224 | anastrozole 1 MG Oral Tablet | SCD | 611e1f43-1442-4cbb-b7eb-b65de15c6c70 | 1 |
Packages#
| Package NDC | 11-digit format | Description | Status |
|---|---|---|---|
| 21695-990-30 | 21695099030 | 30 in 1 BOTTLE | Historical |