ANASTROZOLE
- Product NDC
- 68071-4038
- 11-digit product format
- 680714038
- Labeler code
- 68071
- Product ID
- 68071-4038_69be1c52-93dc-e2c3-e053-2a91aa0af774
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ANASTROZOLE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA079220
- Marketing category
- ANDA
- Marketing start
- 2010-06-28
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ANASTROZOLE
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ANASTROZOLE | 1 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 2Z07MYW1AZ |