Sprintec
- Product NDC
- 21695-769
- 11-digit product format
- 216950769
- Labeler code
- 21695
- Product ID
- 21695-769_e2f5ed4f-dd97-4dda-83d1-f8edd8786c0e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Norgestimate and Ethinyl Estradiol
- Dosage form
- KIT
- Labeler
- Rebel Distributors Corp
- Application
- ANDA075804
- Marketing category
- ANDA
- Marketing start
- 2010-11-22
- Marketing end
- 0000-00-00
- Active strength
- 0
- 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 |
|---|
| 21695-769-28 | Sprintec | 1 in 1 BLISTER PACK | KIT | 1 | | 1 |
| 21695-769-28 | Sprintec | 1 in 1 CARTON | KIT | 1 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-769 | SPRINTEC (NORGESTIMATE AND ETHINYL ESTRADIOL) KIT [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 2 package rows | 20110121_e2f5ed4f-dd97-4dda-83d1-f8edd8786c0e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-769-28 | 21695076928 | 1 in 1 BLISTER PACK | Historical |