Medroxyprogesterone Acetate
- Product NDC
- 0703-6801
- 11-digit product format
- 007036801
- Labeler code
- 0703
- Product ID
- 0703-6801_6a52c8d1-541e-4cb4-b211-f982ce46f0c0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Medroxyprogesterone Acetate
- Dosage form
- INJECTION, SUSPENSION
- Route
- INTRAMUSCULAR
- Labeler
- Teva Parenteral Medicines, Inc.
- 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
- 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 |
|---|
| 0703-6801-01 | 00703680101 | 1 VIAL, SINGLE-DOSE in 1 CARTON (0703-6801-01) > 1 mL in 1 VIAL, SINGLE-DOSE | 2004-09-14 | 0000-00-00 | No | No | Current |
| 0703-6801-04 | 00703680104 | 25 VIAL, SINGLE-DOSE in 1 CARTON (0703-6801-04) > 1 mL in 1 VIAL, SINGLE-DOSE | 2004-09-14 | 0000-00-00 | No | No | Current |