Norethindrone
- Product NDC
- 63187-748
- 11-digit product format
- 631870748
- Labeler code
- 63187
- Product ID
- 63187-748_a55952ea-18c3-4e7b-bb29-16518eae5ff2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Norethindrone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA091209
- Marketing category
- ANDA
- Marketing start
- 2010-11-03
- Substance
- NORETHINDRONE
- Active strength
- .35 mg/1
- Pharmacologic classes
- Progesterone Congeners [CS], Progestin [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Norethindrone
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| NORETHINDRONE | .35 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | T18F433X4S |
| Rxcui | 198042, 748961 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63187-748-28 | Norethindrone | 28 in 1 POUCH | TABLET | 28 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63187-748 | NORETHINDRONE TABLET [PROFICIENT RX LP] | 3 | Current NDC, Legacy NDC, 1 package rows | 20191121_fb84b86e-5f1f-4c17-8b69-ff695c5faf55.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 |
|---|
| 63187-748-28 | 63187074828 | 28 TABLET in 1 POUCH (63187-748-28) | 28 tablet | 2016-10-03 | 0000-00-00 | No | No | Current |