Hydroxyprogesterone Caproate
- Product NDC
- 73301-001
- 11-digit product format
- 733010001
- Labeler code
- 73301
- Product ID
- 73301-001_eb8c444a-ef1b-8f41-e053-2995a90a7025
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxyprogesterone Caproate
- Dosage form
- LIQUID
- Route
- INTRAMUSCULAR
- Labeler
- LSNE, Inc
- Application
- ANDA211777
- Marketing category
- ANDA
- Marketing start
- 2019-08-23
- Marketing end
- 0000-00-00
- Substance
- HYDROXYPROGESTERONE CAPROATE
- Active strength
- 250 mg/mL
- Pharmacologic classes
- Progesterone Congeners [CS], Progestin [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 73301-001-01 | 73301000101 | 1 VIAL, SINGLE-DOSE in 1 BOX (73301-001-01) > 1 mL in 1 VIAL, SINGLE-DOSE | 2019-08-23 | 0000-00-00 | No | No | Current |