Clomiphene Citrate
- Product NDC
- 63629-2165
- 11-digit product format
- 636292165
- Labeler code
- 63629
- Product ID
- 63629-2165_e0a0022e-40f5-4745-96a2-76fb6fd364ee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clomiphene Citrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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 |
|---|
| 63629-2165-1 | 63629216501 | 30 TABLET in 1 BLISTER PACK (63629-2165-1) | 30 tablet | 2022-02-08 | 0000-00-00 | No | No | Current |