HYDROXYPROGESTERONE CAPROATE
- Product NDC
- 55150-309
- 11-digit product format
- 551500309
- Labeler code
- 55150
- Product ID
- 55150-309_4d1b925d-3179-4a37-a48a-440869d599be
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HYDROXYPROGESTERONE CAPROATE
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR
- Labeler
- AuroMedics Pharma LLC
- Application
- ANDA211071
- Marketing category
- ANDA
- Marketing start
- 2019-04-16
- 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
- 2020-12-31
- 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 |
|---|
| 55150-309-01 | 55150030901 | 1 VIAL, SINGLE-DOSE in 1 CARTON (55150-309-01) > 1 mL in 1 VIAL, SINGLE-DOSE | 2019-04-16 | 0000-00-00 | No | No | Current |
| 55150-309-04 | 55150030904 | 4 VIAL, SINGLE-DOSE in 1 CARTON (55150-309-04) > 1 mL in 1 VIAL, SINGLE-DOSE | 2019-04-16 | 0000-00-00 | No | No | Current |