Norethindrone
- Product NDC
- 76413-118
- 11-digit product format
- 764130118
- Labeler code
- 76413
- Product ID
- 76413-118_eaffdcd9-9696-4aeb-b705-3d244ecb9ed8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Norethindrone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Central Texas Community Health Centers
- Application
- ANDA201483
- Marketing category
- ANDA
- Marketing start
- 2013-07-12
- Marketing end
- 0000-00-00
- Substance
- NORETHINDRONE
- Active strength
- 0 mg/1
- Pharmacologic classes
- Progesterone Congeners [CS],Progestin [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 76413-118-28 | Norethindrone | 1 in 1 POUCH | TABLET | 1 | | 1 |
| 76413-118-28 | Norethindrone | 28 in 1 BLISTER PACK | TABLET | 28 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76413-118 | NORETHINDRONE TABLET [CENTRAL TEXAS COMMUNITY HEALTH CENTERS] | 1 | Legacy NDC, 2 package rows | 20160126_3c8baa36-ddf0-46e7-b970-861eb120fce1.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 76413-118-28 | 76413011828 | 1 in 1 POUCH | Historical |