medroxyprogesterone acetate
- Product NDC
- 70518-1932
- 11-digit product format
- 705181932
- Labeler code
- 70518
- Product ID
- 70518-1932_c55cbe0a-2e9b-ace9-e053-2995a90a4139
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- medroxyprogesterone acetate
- Dosage form
- INJECTION, SUSPENSION
- Route
- INTRAMUSCULAR
- Labeler
- REMEDYREPACK INC.
- Application
- NDA020246
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2019-03-04
- Marketing end
- 0000-00-00
- Substance
- MEDROXYPROGESTERONE ACETATE
- Active strength
- 150 mg/mL
- Pharmacologic classes
- Progesterone Congeners [CS],Progestin [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1932-0 | 70518193200 | 1 SYRINGE in 1 CARTON (70518-1932-0) > 1 mL in 1 SYRINGE | 1 syringe | 2019-03-04 | 0000-00-00 | No | No | Current |