Fulvestrant
- Product NDC
- 72603-105
- 11-digit product format
- 726030105
- Labeler code
- 72603
- Product ID
- 72603-105_9f323d55-7d57-4657-a5ad-0748cf7567b4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fulvestrant
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR
- Labeler
- NorthStar Rx LLC
- Application
- ANDA209714
- Marketing category
- ANDA
- Marketing start
- 2019-11-21
- Marketing end
- 0000-00-00
- Substance
- FULVESTRANT
- Active strength
- 50 mg/mL
- Pharmacologic classes
- Estrogen Receptor Antagonist [EPC], Estrogen Receptor Antagonists [MoA], Selective Estrogen Receptor Modulators [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72603-105-02 | 72603010502 | 2 SYRINGE in 1 CARTON (72603-105-02) > 5 mL in 1 SYRINGE (72603-105-01) | 2 syringe | 2019-11-21 | 0000-00-00 | No | No | Current |