Tri-Sprintec
- Product NDC
- 70518-0842
- 11-digit product format
- 705180842
- Labeler code
- 70518
- Product ID
- 70518-0842_e27377d2-bdb9-d1b2-e053-2a95a90ac7c3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- norgestimate and ethinyl estradiol
- Dosage form
- KIT
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075808
- Marketing category
- ANDA
- Marketing start
- 2017-11-10
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-0842 | TRI-SPRINTEC (NORGESTIMATE AND ETHINYL ESTRADIOL) KIT [REMEDYREPACK INC.] | 11 | Legacy NDC | 20241020_666c7d87-cecb-4993-b8ea-a30a773e8129.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0842-0 | 70518084200 | 6 POUCH in 1 CARTON (70518-0842-0) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK | 6 pouch | 2017-11-10 | 0000-00-00 | No | No | Current |