Anastrozole
- Product NDC
- 0093-7536
- 11-digit product format
- 000937536
- Labeler code
- 0093
- Product ID
- 0093-7536_a02eea00-78b1-4cf8-93f7-5d43f59722f0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Anastrozole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA078058
- Marketing category
- ANDA
- Marketing start
- 2010-06-28
- Substance
- ANASTROZOLE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Aromatase Inhibitor [EPC], Aromatase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Anastrozole
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ANASTROZOLE | 1 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 2Z07MYW1AZ |
| Rxcui | 199224 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0093-7536-56 | Anastrozole | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 14 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| ANASTROZOLE | ACTIVE INGREDIENT | 2Z07MYW1AZ | ANASTROZOLE TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 6 | |
| ANASTROZOLE | ACTIVE MOIETY | 2Z07MYW1AZ | ANASTROZOLE TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 6 | |
| HYPROMELLOSE 2910 (5 MPA.S) | INACTIVE INGREDIENT | R75537T0T4 | ANASTROZOLE TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 6 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | ANASTROZOLE TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 6 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | ANASTROZOLE TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 6 | |
| POLYETHYLENE GLYCOL 400 | INACTIVE INGREDIENT | B697894SGQ | ANASTROZOLE TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 6 | |
| POLYETHYLENE GLYCOL 6000 | INACTIVE INGREDIENT | 30IQX730WE | ANASTROZOLE TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 6 | |
| POVIDONE K30 | INACTIVE INGREDIENT | U725QWY32X | ANASTROZOLE TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 6 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | ANASTROZOLE TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 6 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | ANASTROZOLE TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 6 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0093-7536 | ANASTROZOLE TABLET, FILM COATED [TEVA PHARMACEUTICALS USA, INC.] | 14 | Current NDC, Legacy NDC, 1 package rows | 20250412_c58c7013-50a0-4734-8a78-38ff20a3e7eb.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0093-7536-56 | 00093753656 | 30 TABLET, FILM COATED in 1 BOTTLE (0093-7536-56) | 2010-06-28 | 0000-00-00 | No | No | Current |