CLOMIPHENE CITRATE
- Product NDC
- 61919-375
- 11-digit product format
- 619190375
- Labeler code
- 61919
- Product ID
- 61919-375_8385b73e-08c4-d697-e053-2a91aa0a9f8f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CLOMIPHENE CITRATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECTRX
- Application
- ANDA075528
- Marketing category
- ANDA
- Marketing start
- 2019-03-04
- Marketing end
- 0000-00-00
- Substance
- CLOMIPHENE CITRATE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Selective Estrogen Receptor Modulators [MoA],Estrogen Agonist/Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 61919-375-30 | 61919037530 | 30 TABLET in 1 CARTON (61919-375-30) | 30 tablet | 2019-03-04 | 0000-00-00 | No | No | Current |