Estradiol
- Product NDC
- 63187-482
- 11-digit product format
- 631870482
- Labeler code
- 63187
- Product ID
- 63187-482_c6d37f20-6407-4f5b-aecd-8be74fb788cf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Estradiol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA040114
- Marketing category
- ANDA
- Marketing start
- 1996-03-14
- Marketing end
- 0000-00-00
- Substance
- ESTRADIOL
- Active strength
- 1 mg/1
- Pharmacologic classes
- Estradiol Congeners [CS],Estrogen [EPC],Estrogen Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record