MEDROXYPROGESTERONE ACETATE
- Product NDC
- 16714-999
- 11-digit product format
- 167140999
- Labeler code
- 16714
- Product ID
- 16714-999_b6a2702f-2528-4043-89c7-a0a8a5c7cf5c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MEDROXYPROGESTERONE ACETATE
- Dosage form
- INJECTION, SUSPENSION
- Route
- INTRAMUSCULAR
- Labeler
- NorthStar RxLLC
- Application
- ANDA210761
- Marketing category
- ANDA
- Marketing start
- 2019-11-25
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16714-999-01 | 16714099901 | 1 SYRINGE in 1 CARTON (16714-999-01) > 1 mL in 1 SYRINGE | 1 syringe | 2019-11-25 | 0000-00-00 | No | No | Current |