Clomiphene Citrate
- Product NDC
- 50090-0678
- 11-digit product format
- 500900678
- Labeler code
- 50090
- Product ID
- 50090-0678_5302d2b0-24bf-42c6-ab2b-4bc0ae7fcd4a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clomiphene Citrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075528
- Marketing category
- ANDA
- Marketing start
- 1999-08-30
- Marketing end
- 0000-00-00
- Substance
- CLOMIPHENE CITRATE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Estrogen Agonist/Antagonist [EPC], 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 |
|---|
| 50090-0678-0 | 50090067800 | 3 BLISTER PACK in 1 CARTON (50090-0678-0) > 10 TABLET in 1 BLISTER PACK | 3 blister pack | 2018-11-13 | 0000-00-00 | No | No | Current |
| 50090-0678-1 | 50090067801 | 3 BLISTER PACK in 1 CARTON (50090-0678-1) > 10 TABLET in 1 BLISTER PACK | 3 blister pack | 2014-11-28 | 0000-00-00 | No | No | Current |