LEVONORGESTREL
- Product NDC
- 40051-054
- 11-digit product format
- 400510054
- Labeler code
- 40051
- Product ID
- 40051-054_b0fae9d2-a035-152f-e053-2a95a90ad402
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levonorgestrel
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lotus Pharmaceutical Co., Ltd. Nantou Plant
- Application
- ANDA202684
- Marketing category
- ANDA
- Marketing start
- 2020-09-01
- Marketing end
- 2020-10-31
- Substance
- LEVONORGESTREL
- Active strength
- 1 mg/1
- Pharmacologic classes
- Inhibit Ovum Fertilization [PE],Progesterone Congeners [CS],Progesterone Congeners [CS],Progestin [EPC],Progestin-containing Intrauterine Device [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record