Ganirelix Acetate
- Product NDC
- 62756-072
- 11-digit product format
- 627560072
- Labeler code
- 62756
- Product ID
- 62756-072_482153ed-785f-4eb0-9e22-3a608fd0dcc4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ganirelix Acetate
- Dosage form
- INJECTION, SOLUTION
- Route
- SUBCUTANEOUS
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Application
- ANDA204246
- Marketing category
- ANDA
- Marketing start
- 2019-11-07
- Marketing end
- 0000-00-00
- Substance
- GANIRELIX ACETATE
- Active strength
- 250 ug/.5mL
- Pharmacologic classes
- Decreased GnRH Secretion [PE],Gonadotropin Releasing Hormone Antagonist [EPC],Gonadotropin Releasing Hormone Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record