Norethindrone Acetate and Ethinyl Estradiol
- Product NDC
- 70700-101
- 11-digit product format
- 707000101
- Labeler code
- 70700
- Product ID
- 70700-101_0b7a2fac-2281-4c64-29aa-5e0d05d49236
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Norethindrone Acetate and Ethinyl Estradiol Tablets and Ferrous Fumarate Tablets
- Dosage form
- KIT
- Route
- ORAL
- Labeler
- Xiromed, LLC
- Application
- ANDA209609
- Marketing category
- ANDA
- Marketing start
- 2018-08-24
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Norethindrone Acetate and Ethinyl Estradiol
- Listing expiration
- 2026-12-31
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Rxcui | 259176, 1426288, 1426600 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70700-101-85 | Norethindrone Acetate and Ethinyl Estradiol | 1 in 1 BLISTER PACK | KIT | 1 | | 9 |
| 70700-101-85 | Norethindrone Acetate and Ethinyl Estradiol | 3 in 1 CARTON | KIT | 3 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70700-101 | NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL (NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL TABLETS AND FERROUS FUMARATE TABLETS) KIT [XIROMED, LLC] | 9 | Current NDC, Legacy NDC, 2 package rows | 20230722_b4bc4302-9484-465a-090d-47e1e0360b73.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70700-101-85 | 70700010185 | 3 BLISTER PACK in 1 CARTON (70700-101-85) / 1 KIT in 1 BLISTER PACK | 3 blister pack | 2018-08-24 | 0000-00-00 | No | No | Current |