Norepinephrine Bitartrate
- Product NDC
- 0703-1153
- 11-digit product format
- 007031153
- Labeler code
- 0703
- Product ID
- 0703-1153_aba51a00-171e-4dc6-93c2-8e99cdeb8edf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Norepinephrine Bitartrate
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- INTRAVENOUS
- Labeler
- Teva Parenteral Medicines, Inc.
- Application
- ANDA040455
- Marketing category
- ANDA
- Marketing start
- 2021-06-01
- Marketing end
- 0000-00-00
- Substance
- NOREPINEPHRINE BITARTRATE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Catecholamine [EPC],Catecholamines [CS]
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0703-1153-03 | 00703115303 | 10 VIAL, SINGLE-USE in 1 CARTON (0703-1153-03) > 4 mL in 1 VIAL, SINGLE-USE (0703-1153-01) | 2003-04-01 | 0000-00-00 | No | No | Current |
| 0703-1153-83 | 00703115383 | 10 VIAL, SINGLE-USE in 1 CARTON (0703-1153-83) > 4 mL in 1 VIAL, SINGLE-USE (0703-1153-81) | 2021-06-01 | 0000-00-00 | No | No | Current |