Ranitidine
- Product NDC
- 68071-3162
- 11-digit product format
- 680713162
- Labeler code
- 68071
- Product ID
- 68071-3162_bb13ca9a-442b-8fb4-e053-2a95a90a1b5a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA078542
- Marketing category
- ANDA
- Marketing start
- 2008-11-19
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-3162-1 | 68071316201 | 10 TABLET, FILM COATED in 1 BOTTLE (68071-3162-1) | 2017-03-13 | 0000-00-00 | No | No | Current |
| 68071-3162-2 | 68071316202 | 2 TABLET, FILM COATED in 1 BOTTLE (68071-3162-2) | 2017-03-13 | 0000-00-00 | No | No | Current |
| 68071-3162-6 | 68071316206 | 6 TABLET, FILM COATED in 1 BOTTLE (68071-3162-6) | 2017-03-13 | 0000-00-00 | No | No | Current |