Clomiphene Citrate
- Product NDC
- 21695-114
- 11-digit product format
- 216950114
- Labeler code
- 21695
- Product ID
- 21695-114_49860a2f-92f2-4da8-b78f-0efc005d725a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clomiphene Citrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- 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
- Selective Estrogen Receptor Modulators [MoA],Estrogen Agonist/Antagonist [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 21695-114-10 | Clomiphene Citrate | 10 in 1 BLISTER PACK | TABLET | 10 | | 1 |
| 21695-114-10 | Clomiphene Citrate | 1 in 1 CARTON | TABLET | 1 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-114 | CLOMIPHENE CITRATE TABLET [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 2 package rows | 20101123_49860a2f-92f2-4da8-b78f-0efc005d725a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-114-10 | 21695011410 | 10 in 1 BLISTER PACK | Historical |