Fulvestrant
- Product NDC
- 0310-7720
- 11-digit product format
- 003107720
- Labeler code
- 0310
- Product ID
- 0310-7720_45b2245b-9f11-4b58-a275-b664b5b89e7d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fulvestrant
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR
- Labeler
- AstraZeneca Pharmaceuticals LP
- Application
- NDA021344
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2019-10-08
- Marketing end
- 2023-03-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0310-7720-10 | 00310772010 | 2 SYRINGE, GLASS in 1 CARTON (0310-7720-10) > 5 mL in 1 SYRINGE, GLASS | 2019-10-08 | 2023-03-31 | No | No | Current |