Cryselle
- Product NDC
- 71205-803
- 11-digit product format
- 712050803
- Labeler code
- 71205
- Product ID
- 71205-803_9c4fac8e-8744-4378-80af-7887de955a51
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Norgestrel and Ethinyl Estradiol
- Dosage form
- KIT
- Labeler
- Proficient Rx LP
- Application
- ANDA075840
- Marketing category
- ANDA
- Marketing start
- 2002-07-24
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Cryselle
- Listing expiration
- 2026-12-31
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Rxcui | 311359, 748797, 749786, 750265 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71205-803-28 | Cryselle | 1 in 1 POUCH | KIT | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-803 | CRYSELLE (NORGESTREL AND ETHINYL ESTRADIOL) KIT [PROFICIENT RX LP] | 1 | Current NDC, 1 package rows | 20230531_9c4fac8e-8744-4378-80af-7887de955a51.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71205-803-28 | 71205080328 | 1 KIT in 1 POUCH (71205-803-28) | 1 kit | 2023-05-30 | No | No | Current |