AMPICILLIN
- Product NDC
- 0404-9816
- 11-digit product format
- 004049816
- Labeler code
- 0404
- Product ID
- 0404-9816_eea94eb1-b337-4536-abbd-66eb95a488f9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMPICILLIN SODIUM
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Henry Schein, Inc.
- Application
- ANDA065499
- Marketing category
- ANDA
- Marketing start
- 2022-01-08
- Marketing end
- 0000-00-00
- Substance
- AMPICILLIN SODIUM
- Active strength
- 1 g/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC], Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 0404-9816 | AMPICILLIN (AMPICILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [HENRY SCHEIN, INC.] | 5 | Legacy NDC | 20241105_294b2a06-695d-4f51-99e4-248b772db55c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0404-9816-99 | 00404981699 | 1 VIAL in 1 BAG (0404-9816-99) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL | 1 vial | 2022-01-08 | 0000-00-00 | No | No | Current |