Progesterone Injection
- Product NDC
- 40042-050
- 11-digit product format
- 400420050
- Labeler code
- 40042
- Product ID
- 40042-050_dc3647a7-842f-46ab-8b42-d19e66a251e9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Progesterone Injection
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR
- Labeler
- PharmaForce, Inc.
- Application
- ANDA090845
- Marketing category
- ANDA
- Marketing start
- 2009-09-04
- Marketing end
- 0000-00-00
- Substance
- PROGESTERONE
- Active strength
- 50 mg/mL
- Pharmacologic classes
- Progesterone [CS],Progesterone [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#