Medroxyprogesterone Acetate
- Product NDC
- 71205-118
- 11-digit product format
- 712050118
- Labeler code
- 71205
- Product ID
- 71205-118_5655db41-00a4-41ec-a253-b6d0d3a22e94
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Medroxyprogesterone Acetate
- Dosage form
- INJECTION, SUSPENSION
- Route
- INTRAMUSCULAR
- Labeler
- Proficient Rx LP
- Application
- ANDA076553
- Marketing category
- ANDA
- Marketing start
- 2004-09-14
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-118 | MEDROXYPROGESTERONE ACETATE INJECTION, SUSPENSION [PROFICIENT RX LP] | 3 | Legacy NDC | 20191115_9451ca1a-34a4-46e2-bacc-6268a2f60bc8.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-118-01 | 71205011801 | 1 VIAL, SINGLE-DOSE in 1 CARTON (71205-118-01) > 1 mL in 1 VIAL, SINGLE-DOSE | 2018-09-04 | 0000-00-00 | No | No | Current |