Norethindrone
- Product NDC
- 70518-3113
- 11-digit product format
- 705183113
- Labeler code
- 70518
- Product ID
- 70518-3113_c445026a-492a-7b72-e053-2995a90a9fa8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Norethindrone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA200980
- Marketing category
- ANDA
- Marketing start
- 2021-06-08
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3113-0 | 70518311300 | 3 POUCH in 1 CARTON (70518-3113-0) > 1 BLISTER PACK in 1 POUCH > 28 TABLET in 1 BLISTER PACK | 3 pouch | 2021-06-08 | 0000-00-00 | No | No | Current |