Ranitidine
- Product NDC
- 70000-0033
- 11-digit product format
- 700000033
- Labeler code
- 70000
- Product ID
- 70000-0033_3eae53a8-c3bf-455b-f5f6-a73e2c827133
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- CARDINAL HEALTH
- Application
- ANDA075294
- Marketing category
- ANDA
- Marketing start
- 2019-05-28
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 75 mg/1
- Pharmacologic classes
- Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70000-0033-1 | 70000003301 | 1 BOTTLE in 1 CARTON (70000-0033-1) > 30 TABLET in 1 BOTTLE | 1 bottle | 2019-05-28 | 0000-00-00 | No | No | Current |
| 70000-0033-2 | 70000003302 | 1 BOTTLE in 1 CARTON (70000-0033-2) > 80 TABLET in 1 BOTTLE | 1 bottle | 2019-05-28 | 0000-00-00 | No | No | Current |