Ampicillin
- Product NDC
- 36000-070
- 11-digit product format
- 360000070
- Labeler code
- 36000
- Product ID
- 36000-070_0bfd0e69-f2ec-4ce6-a97d-e0812c65c27b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ampicillin sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Claris Lifesciences, Inc.
- Application
- ANDA090354
- Marketing category
- ANDA
- Marketing start
- 2010-04-25
- Marketing end
- 0000-00-00
- Substance
- AMPICILLIN SODIUM
- Active strength
- 250 mg/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 36000-070-10 | Ampicillin | 10 in 1 CARTON | INJECTION, POWDER, FOR SOLUTION | 10 | | 3 |
| 36000-070-10 | Ampicillin | 1 in 1 VIAL | INJECTION, POWDER, FOR SOLUTION | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 36000-070 | AMPICILLIN (AMPICILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION AMPICILLIN (AMPICILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [CLARIS LIFESCIENCES, INC.] | 3 | Legacy NDC, 2 package rows | 20100426_da8da9c0-fa46-40d3-82c6-1a18ffa1b585.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 36000-070-10 | 36000007010 | 10 in 1 CARTON | Historical |